Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytesJACKY, P. B; AHUJA, Y. R; HOLMGREN, G et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 400-403, issn 0148-7299Article

Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaicNIENELTOW, M; COOPER, M; BREG, W. R et al.Cancer genetics and cytogenetics. 1984, Vol 12, Num 3, pp 261-265, issn 0165-4608Article

Molecular and cytogenetic characterization of 9p-abnormalitiesTEEBI, A. S; GIBSON, L; MCGRATH, J et al.American journal of medical genetics. 1993, Vol 46, Num 3, pp 288-292, issn 0148-7299Article

Chromosome deletion 1q42-43WATSON, M. S; GARGUS, J. J; BLAKEMORE, K. J et al.American journal of medical genetics. 1986, Vol 24, Num 1, pp 1-6, issn 0148-7299Article

NRAS transforming gene maps to region p11→p13 on chromosome 1 by in situ hybridizationRABIN, M; WATSON, M; BARKER, P. E et al.Cytogenetics and cell genetics. 1984, Vol 38, Num 1, pp 70-72, issn 0301-0171Article

Prenatal detection of two different monosomic cell lines by chorionic villus samplingHSU, T.-Y; LIOU, J.-D; COPEL, J. A et al.Prenatal diagnosis. 1996, Vol 16, Num 2, pp 169-172, issn 0197-3851Article

FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotypeCHU, T. W; TEEBI, A. S; GIBSON, L et al.American journal of medical genetics. 1994, Vol 52, Num 1, pp 92-96, issn 0148-7299Article

Fetal blood sampling and cytogenetic abnormalitiesJUI-DER LIOU; CHIH-PING CHEN; BREG, W. R et al.Prenatal diagnosis. 1993, Vol 13, Num 1, pp 1-8, issn 0197-3851Article

A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autismPAUL, R; DYKENS, E; LECKMAN, J. F et al.Journal of autism and developmental disorders. 1987, Vol 17, Num 4, pp 457-468, issn 0162-3257Article

Human c-fos oncogene mapped within chromosomal region 14q21→q31BARKER, P. E; RABIN, M; WATSON, M et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 18, pp 5826-5830, issn 0273-1134Article

Anthropometric and craniofacial patterns in mentally retarted males with emphasis on the fragile X syndromeBUTLER, M. G; PRATESI, R; WATSON, M. S et al.Clinical genetics. 1993, Vol 44, Num 3, pp 129-138, issn 0009-9163Article

Anthropometric comparison of mentally retarded males with and without the fragile X syndromeBUTLER, M. G; ALLEN, G. A; HAYNES, J. L et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 260-268, issn 0148-7299Article

Duplication of euchromatin without phenotypic effects : a variant of chromosome 16BRYKE, C. R; BREG, W. R; POTLURI, V. R et al.American journal of medical genetics. 1990, Vol 36, Num 1, pp 43-44, issn 0148-7299, 2 p.Article

Report of two cases of distal deletion of the long arm of chromosome 6STEVENS, C. A; FINEMAN, R. M; BREG, W. R et al.American journal of medical genetics. 1988, Vol 29, Num 4, pp 807-814, issn 0148-7299Article

Regional location of α₁-antichymotrypsin and α₁-antitrypsin genes on human chromosome 14RABIN, M; WATSON, M; KIDD, V et al.Somatic cell and molecular genetics. 1986, Vol 12, Num 2, pp 209-214, issn 0740-7750Article

Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq-karyotypeLAHN, B. T; MA, N; BREG, W. R et al.Nature genetics. 1994, Vol 8, Num 3, pp 243-250, issn 1061-4036Article

Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)PETTY, E. M; GIBSON, L. H; BREG, W. R et al.American journal of medical genetics. 1993, Vol 45, Num 6, pp 770-773, issn 0148-7299Article

Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataWERTELECKI, W; BREG, W. R; GRAHAM, S. M. JR et al.American journal of medical genetics. 1986, Vol 23, Num 3, pp 739-749, issn 0148-7299Article

Fragile X syndrome: its relations to speech and language disordersPAUL, R; COHEN, D. J; BREG, W. R et al.The Journal of speech and hearing disorders. 1984, Vol 49, Num 3, pp 328-332, issn 0022-4677Article

Familial occurrence of esophageal atresia with and without tracheoesophageal fistula : report of two unusual kindredsPLETCHER, B. A; FRIEDES, J. S; BREG, W. R et al.American journal of medical genetics. 1991, Vol 39, Num 4, pp 380-384, issn 0148-7299, 5 p.Article

DNA-based genetic testing in fifty fragile X familiesMURPHY, P. D; WATSON, M. S; SHAPIRO, L. R et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 305-310, issn 0148-7299Article

Pseudomosaicism for 4p-in amniotic fluid cell culture proven to be true mosaicism after birthVOCKLEY, J; INSERRA, J; BREG, W. R et al.American journal of medical genetics. 1991, Vol 39, Num 1, pp 81-83, issn 0148-7299Article

Deletion (12) (q 15 q 21.2)WATSON, M. S; MCALLISTER-BARTON, L; MAHONEY, M. J et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 343-344, issn 0022-2593, 2 p.Article

Cytogenetic diagnosis using midtrimester fetal blood samples: application to suspected mosaicism and other diagnostic problemsWATSON, M. S; BREG, W. R; HOBBINS, J. C et al.American journal of medical genetics. 1984, Vol 19, Num 4, pp 805-813, issn 0148-7299Article

Fetal cystic hygroma. Cause and natural historyCHERVENAK, F. A; ISAACSON, G; BLAKEMORE, K. J et al.The New England journal of medicine. 1983, Vol 309, Num 14, pp 822-825, issn 0028-4793Article