• 45551 Citations
  • 100 Scopus h-Index
1978 …2021
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Research Output 1978 2019

  • 45551 Citations
  • 100 Scopus h-Index
  • 491 Article
  • 4 Chapter
  • 4 Comment/debate
  • 1 Review article
1996
2 Citations (Scopus)

A polymerase chain reaction-based test for spinal and bulbar muscular atrophy

Wang, Z. & Thibodeau, S. N., 1996, In : Mayo Clinic Proceedings. 71, 4, p. 397-398 2 p.

Research output: Contribution to journalArticle

Atrophic Muscular Disorders
Polymerase Chain Reaction
Thalassemia
Globins
Terminator Codon
Genes
Mutation

Erratum: Frequent loss of heterozygosity at 7q31.1 is associated with tumor aggressiveness and progression (Cancer Research (September 15, 1995) 55 (4114-4119))

Takahashi, S., Shan, A. L., Ritland, S. R., Delacey, K. A., Bostwick, D. G., Lieber, M. M., Thibodeau, S. N. & Jenkins, R. B., 1996, In : Cancer Research. 56, 10, p. 2461 1 p.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Research
Neoplasms
3 Citations (Scopus)

Hb Cook [β132(H10)Lys→Thr]: A new hemoglobin variant in a southeast Asian family

Hutt, P. J., Fairbanks, V. F., Griffin, T. C., Thibodeau, S. N., Green, M. M. & Hoyer, J., 1996, In : Hemoglobin. 20, 4, p. 371-376 6 p.

Research output: Contribution to journalArticle

Hemoglobins
Globins
DNA Sequence Analysis
Codon
Genes
8 Citations (Scopus)

Hemoglobin S/hemoglobin Osler: A case with 3 β globin chains. DNA sequence (AAT) proves that Hb Osler is β 145 Tyr→Asn

Hutt, P. J., Donaldson, M. H., Khatri, J., Fairbanks, V. F., Hoyer, J., Thibodeau, S. N., Moxness, M. S., McMorrow, L. E., Green, M. M. & Jones, R. T., 1996, In : American Journal of Hematology. 52, 4, p. 305-309 5 p.

Research output: Contribution to journalArticle

Sickle Hemoglobin
Globins
Codon
Electrophoresis
Exons
222 Citations (Scopus)

Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer

Moslein, G., Tester, D. J., Lindor, N. M., Honchel, R., Cunningham, J. M., French, A. J., Halling, K. C., Schwab, M., Goretzki, P. & Thibodeau, S. N., Sep 1996, In : Human Molecular Genetics. 5, 9, p. 1245-1252 8 p.

Research output: Contribution to journalArticle

Microsatellite Instability
Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms
Mutation
DNA Mismatch Repair
17 Citations (Scopus)

p53 functional loss in a colon cancer cell line with two missense mutations (2181eu and 248trp) on separate alleles

Rand, A., Glenn, K. S., Alvares, C. P., White, M. B., Thibodeau, S. N. & Karnes, W. E., Jan 2 1996, In : Cancer Letters. 98, 2, p. 183-191 9 p.

Research output: Contribution to journalArticle

Missense Mutation
Colonic Neoplasms
Alleles
Cell Line
Valine
1094 Citations (Scopus)

Preclinical evidence of Alzheimer's disease in persons homozygous for the ε4 allele for apolipoprotein E

Reiman, E. M., Caselli, R. J., Yun, L. S., Chen, K., Bandy, D., Minoshima, S., Thibodeau, S. N. & Osborne, D., Mar 21 1996, In : New England Journal of Medicine. 334, 12, p. 752-758 7 p.

Research output: Contribution to journalArticle

Apolipoprotein E4
Alzheimer Disease
Alleles
Positron-Emission Tomography
Glucose
59 Citations (Scopus)

Predictive value of APOE genotyping in incipient Alzheimer's disease

Petersen, R. C., Waring, S. C., Smith, G. E., Tangalos, E. G. & Thibodeau, S. N., 1996, In : Annals of the New York Academy of Sciences. 802, p. 58-69 12 p.

Research output: Contribution to journalArticle

Apolipoproteins E
Apolipoprotein E4
Dementia
Alzheimer Disease
Data storage equipment
68 Citations (Scopus)

Rothmund-Thomson syndrome in siblings: Evidence for acquired in vivo mosaicism

Lindor, N. M., Devries, E. M. G., Michels, V. V., Schad, C. R., Jalal, S. M., Donovan, K. M., Smithson, W. A., Kvols, L. K., Thibodeau, S. N. & Dewald, G. W., Mar 1996, In : Clinical Genetics. 49, 3, p. 124-129 6 p.

Research output: Contribution to journalArticle

Rothmund-Thomson Syndrome
Mosaicism
Siblings
Cytogenetics
Clone Cells
6 Citations (Scopus)

Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus

Kambouris, M., Snow, K., Thibodeau, S. N., Bluhm, D., Green, M. & Feldman, G. L., Aug 9 1996, In : American Journal of Medical Genetics. 64, 2, p. 404-407 4 p.

Research output: Contribution to journalArticle

Alleles
Mutation
Methylation
Mothers
Nuclear Family
133 Citations (Scopus)

The premortem recognition of systemic senile amyloidosis with cardiac involvement

Kyle, R. A., Spittell, P. C., Gertz, M., Li, C. Y., Edwards, W. D., Olson, L. J. & Thibodeau, S. N., Oct 1996, In : American Journal of Medicine. 101, 4, p. 395-400 6 p.

Research output: Contribution to journalArticle

Amyloidosis
Prealbumin
Familial Amyloidosis
Amyloid
Immune Sera
918 Citations (Scopus)

The relationship between specific ret proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET mutation consortium analysis

Eng, C., Clayton, D., Schuffenecker, I., Lenoir, G., Cote, G., Gagel, R. F., Ploos Van Amstel, H. K., Lips, C. J. M., Nishisho, I., Takai, S. I., Marsh, D. J., Robinson, B. G., Frank-Raue, K., Raue, F., Xue, F., Noll, W. W., Romei, C., Pacini, F., Fink, M., Niederle, B. & 10 others, Zedenius, J., Nordenskjöld, M., Komminoth, P., Hendy, G. N., Gharib, H., Thibodeau, S. N., Lacroix, A., Frilling, A., Ponder, B. A. J. & Mulligan, L. M., Nov 20 1996, In : Journal of the American Medical Association. 276, 19, p. 1575-1579 5 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 2a
Proto-Oncogenes
Phenotype
Mutation
Codon
50 Citations (Scopus)

Tumor necrosis factor-α allelic frequency and chromosome 6 allelic imbalance in patients with colorectal cancer

Honchel, R., McDonnell, S., Schaid, D. J. & Thibodeau, S. N., Jan 1 1996, In : Cancer Research. 56, 1, p. 145-149 5 p.

Research output: Contribution to journalArticle

Allelic Imbalance
Chromosomes, Human, Pair 6
Loss of Heterozygosity
Colorectal Neoplasms
Tumor Necrosis Factor-alpha
1995
76 Citations (Scopus)

A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis

Olson, T. M., Michels, V. V., Urban, Z., Csiszar, K., Christiano, A. M., Driscoll, D. J., Feldt, R. H., Boyd, C. D. & Thibodeau, S. N., 1995, In : Human Molecular Genetics. 4, 9, p. 1677-1679 3 p.

Research output: Contribution to journalArticle

Molecular Sequence Data
Aortic Stenosis
Supravalvular Aortic Stenosis
Elastin
Sequence Deletion
649 Citations (Scopus)

Apolipoprotein E status as a predictor of the development of Alzheimer's disease in memory-impaired individuals

Petersen, R. C., Smith, G. E., Ivnik, R. J., Tangalos, E. G., Schaid, D. J., Thibodeau, S. N., Tangalos, E. G., Schaid, D. J. & Thibodeau, S. N., 1995, In : Journal of the American Medical Association. 273, 16, p. 1274-1278 5 p.

Research output: Contribution to journalArticle

Apolipoproteins E
Alzheimer Disease
Apolipoprotein E4
Dementia
Wechsler Scales
8 Citations (Scopus)

Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathy

Olson, T. M., Thibodeau, S. N., Lundquist, P. A., Schaid, D. J. & Michels, V. V., 1995, In : Journal of Medical Genetics. 32, 11, p. 876-880 5 p.

Research output: Contribution to journalArticle

Dilated Cardiomyopathy
exclusion
Disease
Penetrance
Genes
16 Citations (Scopus)

Familial medullary thyroid cancer and prominent corneal nerves: Clinical and genetic analysis

Kane, L. A., Tsai, M. S., Gharib, H., Khosla, S., Robertson, D. M., Schaid, D. J., Honchel, R. & Thibodeau, S. N., 1995, In : Journal of Clinical Endocrinology and Metabolism. 80, 1, p. 289-293 5 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia
DNA sequences
Exons
Pentagastrin
Calcitonin
127 Citations (Scopus)

Frequent loss of heterozygosity at 7q31.1 in primary prostate cancer is associated with tumor aggressiveness and progression

Takahashi, S., Shan, A. L., Ritland, S. R., Delacey, K. A., Bostwick, D. G., Lieber, M. M., Thibodeau, S. N. & Jenkins, R. B., 1995, In : Cancer Research. 55, 18, p. 4114-4119 6 p.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Chromosomes, Human, Pair 7
Allelic Imbalance
Prostatic Neoplasms
Neoplasms
2 Citations (Scopus)

Genetic testing for Prader-Willi and Angelman syndromes

Schad, C. R., Jalal, S. M. & Thibodeau, S. N., 1995, In : Mayo Clinic Proceedings. 70, 12, p. 1195-1196 2 p.

Research output: Contribution to journalArticle

Angelman Syndrome
Prader-Willi Syndrome
Genetic Testing
84 Citations (Scopus)

Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II

Ledger, G. A., Khosla, S., Lindor, N. M., Thibodeau, S. N. & Gharib, H., 1995, In : Annals of Internal Medicine. 122, 2, p. 118-124 7 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia
Genetic Testing
Pentagastrin
Information Storage and Retrieval
Calcitonin
77 Citations (Scopus)

Genomic instability in neoplasia

Honchel, R., Halling, K. C. & Thibodeau, S. N., 1995, In : Seminars in Cell Biology. 6, 1, p. 45-52 8 p.

Research output: Contribution to journalArticle

Genomic Instability
Microsatellite Instability
Hereditary Nonpolyposis Colorectal Neoplasms
DNA Mismatch Repair
Neoplasms
231 Citations (Scopus)

Genotype-phenotype correlation in multiple endocrine neoplasia type 2: Report of the International RET Mutation Consortium

Mulligan, L. M., Marsh, D. J., Robinson, B. G., Schuffenecker, I., Zedenius, J., Lips, C. J. M., Gagel, R. F., Takai, S. I., Noll, W. W., Fink, M., Raue, F., Lacroix, A., Thibodeau, S. N., Frilling, A., Ponder, B. A. J. & Eng, C., 1995, In : Journal of Internal Medicine. 238, 4, p. 343-346 4 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 2a
Genetic Association Studies
Mutation
Multiple Endocrine Neoplasia Type 2b
Multiple Endocrine Neoplasia
28 Citations (Scopus)

Microsatellite instability in keratoacanthoma

Halling, K. C., Honchel, R., Pittelkow, M. R. & Thibodeau, S. N., 1995, In : Cancer. 76, 10, p. 1765-1771 7 p.

Research output: Contribution to journalArticle

Keratoacanthoma
Microsatellite Instability
Muir-Torre Syndrome
Hereditary Nonpolyposis Colorectal Neoplasms
DNA Mismatch Repair
61 Citations (Scopus)

Mutations in the RET protooncogene in sporadic pheochromocytomas

Lindor, N. M., Honchel, R., Khosla, S. & Thibodeau, S. N., 1995, In : Journal of Clinical Endocrinology and Metabolism. 80, 2, p. 627-629 3 p.

Research output: Contribution to journalArticle

Pheochromocytoma
Exons
Mutation
Tumors
Multiple Endocrine Neoplasia
59 Citations (Scopus)

The fragile X premutation in carriers and its effect on mutation size in offspring

Fisch, G. S., Snow, K., Thibodeau, S. N., Chalifaux, M., Holden, J. J. A., Nelson, D. L., Howard-Peebles, P. N. & Maddalena, A., 1995, In : American Journal of Human Genetics. 56, 5, p. 1147-1155 9 p.

Research output: Contribution to journalArticle

Mutation
Nuclear Family
Mothers
Trinucleotide Repeats
Fragile X Syndrome
31 Citations (Scopus)

Transthyretin Ser 6 gene frequency in individuals without amyloidosis

Jacobson, D. R., Alves, I. L., Saraiva, M. J., Thibodeau, S. N. & Buxbaum, J. N., Mar 1995, In : Human Genetics. 95, 3, p. 308-312 5 p.

Research output: Contribution to journalArticle

Prealbumin
Amyloidosis
Gene Frequency
African Americans
Familial Amyloidosis
12 Citations (Scopus)

Uniparental disomy in congenital disorders: A prospective study

Lindor, N. M., Karnes, P. S., Michels, V. V., Dewald, G. W., Goerss, J., Jalal, S., Jenkins, R. B., Vockley, G. & Thibodeau, S. N., 1995, In : American Journal of Medical Genetics. 58, 2, p. 143-146 4 p.

Research output: Contribution to journalArticle

Uniparental Disomy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Prospective Studies
Chromosomes
Intellectual Disability
1994
234 Citations (Scopus)

Apolipoprotein E: Risk factor for Alzheimer disease

Tsai, M. S., Tangalos, E. G., Petersen, R. C., Smith, G. E., Schaid, D. J., Kokmen, E., Ivnik, R. J. & Thibodeau, S. N., 1994, In : American Journal of Human Genetics. 54, 4, p. 643-649 7 p.

Research output: Contribution to journalArticle

Apolipoproteins E
Alzheimer Disease
Apolipoprotein E4
Alleles
Genes
29 Citations (Scopus)

Apolipoprotein E allele in Chamorros with amyotrophic lateral sclerosis/parkinsonism-dementia complex

Waring, S. C., O'Brien, P. C., Kurland, L. T., Thibodeau, S. N., Tsai, M. S., Petersen, R. C. & Esteban-Santillan, C. E., Mar 5 1994, In : The Lancet. 343, 8897, p. 611 1 p.

Research output: Contribution to journalArticle

Guam
Amyotrophic Lateral Sclerosis
Parkinsonian Disorders
Apolipoproteins E
Parkinson Disease
27 Citations (Scopus)

Circulating heart autoantibodies in familial as compared with nonfamilial idiopathic dilated cardiomyopathy

Michels, V. V., Moll, P. P., Rodeheffer, R. J., Miller, F. A. J., Tajik, A. J., Burnett, J. C. J., Driscoll, D. J., Thibodeau, S. N., Ansari, A. A. & Herskowitz, A., 1994, In : Mayo Clinic Proceedings. 69, 1, p. 24-27 4 p.

Research output: Contribution to journalArticle

Dilated Cardiomyopathy
Autoantibodies
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Cardiac Myosins
Ventricular Dysfunction
11 Citations (Scopus)

Confirmation of linkage of supravalvular aortic stenosis to the elastin gene on chromosome 7q

Kumar, A., Olson, T. M., Thibodeau, S. N., Michels, V. V., Schaid, D. J. & Wallace, M. R., Dec 15 1994, In : The American Journal of Cardiology. 74, 12, p. 1281-1283 3 p.

Research output: Contribution to journalArticle

Supravalvular Aortic Stenosis
Elastin
Chromosomes
Genetic Heterogeneity
Genes
167 Citations (Scopus)

High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression

Hagerman, R. J., Hull, C. E., Safanda, J. F., Carpenter, I., Staley, L. W., O'Connor, R. A., Seydel, C., Mazzocco, M. M. M., Snow, K., Thibodeau, S. N., Kuhl, D., Nelson, D. L., Caskey, C. T. & Taylor, A. K., 1994, In : American Journal of Medical Genetics. 51, 4, p. 298-308 11 p.

Research output: Contribution to journalArticle

Mutation
Proteins
DNA
Cytogenetics
Methylation
47 Citations (Scopus)

Identification of multiple endocrine neoplasia, type 2 gene carriers using linkage analysis and analysis of the RET proto-oncogene

Tsai, M. S., Ledger, G. A., Khosla, S., Gharib, H. & Thibodeau, S. N., May 1994, In : Journal of Clinical Endocrinology and Metabolism. 78, 5, p. 1261-1264 4 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 2a
Proto-Oncogenes
Genes
Exons
DNA sequences
380 Citations (Scopus)

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

Eichler, E. E., Holden, J. J. A., Popovich, B. W., Reiss, A. L., Snow, K., Thibodeau, S. N., Richards, C. S., Ward, P. A. & Nelson, D. L., Sep 1994, In : Nature Genetics. 8, 1, p. 88-94 7 p.

Research output: Contribution to journalArticle

Alleles
Fragile X Syndrome
Genes
Chromosomes, Human, X
167 Citations (Scopus)

Microsatellite instability in Muir-Torre syndrome

Honchel, R., Hailing, K. C., Schaid, D. J., Thibodeau, S. N. & Thibodeau, S. N., Mar 1 1994, In : Cancer Research. 54, 5, p. 1159-1163 5 p.

Research output: Contribution to journalArticle

Muir-Torre Syndrome
Microsatellite Instability
Colorectal Neoplasms
Neoplasms
Carcinogenesis

Mutator gene effect in colorectal cancer

Thibodeau, S. N., 1994, In : Clinical Chemistry. 40, 4, p. 638 1 p.

Research output: Contribution to journalArticle

Colorectal Neoplasms
Genes
4 Citations (Scopus)

Recent applications of PCR in clinical laboratory medicine.

Thibodeau, S. N., May 1994, In : Clinical Chemistry. 40, 5, p. 681-682 2 p.

Research output: Contribution to journalArticle

Clinical laboratories
Clinical Medicine
Polymerase chain reaction
Medicine
Polymerase Chain Reaction
8 Citations (Scopus)

Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing

Fisch, G. S., Nelson, D. L., Snow, K., Thibodeau, S. N., Chalifoux, M. & Holden, J. J. A., 1994, In : American Journal of Medical Genetics. 51, 4, p. 339-345 7 p.

Research output: Contribution to journalArticle

Fragile X Syndrome
Alleles
DNA
Population
Normal Distribution
7 Citations (Scopus)

Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenics

Lindor, N. M., Sobell, J. L., Heston, L. L., Thibodeau, S. N. & Sommer, S. S., 1994, In : American Journal of Medical Genetics. 54, 1, p. 1-4 4 p.

Research output: Contribution to journalArticle

Dystrophin
Viverridae
Schizophrenia
Genes
Duchenne Muscular Dystrophy
140 Citations (Scopus)

Sequence analysis of the fragile X trinucleotide repeat: Implications for the origin of the fragile X mutation

Snow, K., Tester, D. J., Kruckeberg, K. E., Schaid, D. J. & Thibodeau, S. N., Sep 1994, In : Human Molecular Genetics. 3, 9, p. 1543-1551 9 p.

Research output: Contribution to journalArticle

Trinucleotide Repeats
Sequence Analysis
Ferromagnetic resonance
Mutation
Alleles
556 Citations (Scopus)

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

Mulligan, L. M., Eng, C., Healey, C. S., Clayton, D., Kwok, J. B. J., Gardner, E., Ponder, M. A., Frilling, A., Jackson, C. E., Lehnert, H., Neumann, H. P. H., Thibodeau, S. N. & Ponder, B. A. J., Jan 1994, In : Nature Genetics. 6, 1, p. 70-74 5 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 2a
Proto-Oncogenes
Phenotype
Multiple Endocrine Neoplasia Type 2b
Mutation
1993
185 Citations (Scopus)

Analysis of a CGG sequence at the FMR-I locus in fragile X families and in the general population

Snow, K., Doud, L. K., Hagerman, R., Pergolizzi, R. G., Erster, S. H. & Thibodeau, S. N., Dec 1993, In : American Journal of Human Genetics. 53, 6, p. 1217-1228 12 p.

Research output: Contribution to journalArticle

Southern Blotting
Alleles
Polymerase Chain Reaction
Mutation
Methylation
50 Citations (Scopus)

Autosomal dominant supravalvular aortic stenosis: Localization to chromosome 7

Olson, T. M., Michels, V. V., Lindor, N. M., Pastores, G. M., Weber, J. L., Schaid, D. J., Driscoll, D. J., Feldt, R. H. & Thibodeau, S. N., Jul 1993, In : Human Molecular Genetics. 2, 7, p. 869-873 5 p.

Research output: Contribution to journalArticle

Aortic Stenosis
Supravalvular Aortic Stenosis
Chromosomes, Human, Pair 7
Chromosomes
Chromosome
18 Citations (Scopus)

Dystrophin analysis in idiopathic dilated cardiomyopathy

Michels, V. V., Pastores, G. M., Moll, P. P., Driscoll, D. J., Miller, F. A. J., Burnett, J. C. J., Rodeheffer, R. J., Tajik, J. A., Beggs, A. H., Kunkel, L. M. & Thibodeau, S. N., 1993, In : Journal of Medical Genetics. 30, 11, p. 955-957 3 p.

Research output: Contribution to journalArticle

Dystrophin
Dilated Cardiomyopathy
Genes
Muscle Cramp
Duchenne Muscular Dystrophy
3 Citations (Scopus)

Eight novel polymorphisms in the dystrophin gene of African-Americans: The rate of polymorphism is high

Lindor, N. M., Sommer, S. S., Sobell, J., Heston, L. & Thibodeau, S. N., 1993, In : Human Mutation. 2, 6, p. 485-488 4 p.

Research output: Contribution to journalArticle

Dystrophin
Southern Blotting
Restriction Fragment Length Polymorphisms
African Americans
Genes
2617 Citations (Scopus)

Microsatellite instability in cancer of the proximal colon

Thibodeau, S. N., Bren, G. & Schaid, D. J., 1993, In : Science. 260, 5109, p. 816-819 4 p.

Research output: Contribution to journalArticle

Microsatellite Instability
Colonic Neoplasms
Loss of Heterozygosity
Colorectal Neoplasms
Neoplasms
22 Citations (Scopus)

Molecular-clinical correlations in children and adults with fragile X syndrome

Staley, L. W., Hull, C. E., Mazzocco, M. M. M., Thibodeau, S. N., Snow, K., Wilson, V. L., Taylor, A., McGavran, L., Weiner, D., Riddle, J., O'Connor, R. & Hagerman, R. J., 1993, In : American Journal of Diseases of Children. 147, 7, p. 723-726 4 p.

Research output: Contribution to journalArticle

Fragile X Syndrome
Intellectual Disability
Guanine
Mutation
Aptitude
32 Citations (Scopus)

Mosaic trisomy 16 in a thriving infant; maternal heterodisomy for chromosome 16

Lindor, N. M., Jalal, S. M., Thibodeau, S. N., Bonde, D., Sauser, K. L. & Karnes, P. S., 1993, In : Clinical Genetics. 44, 4, p. 185-189 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Mothers
Mosaicism
Karyotype
Fibroblasts

News and comments

Thibodeau, S. N., 1993, In : Diseases of the Colon and Rectum. 36, 8, p. 727 1 p.

Research output: Contribution to journalArticle