Positional cloning moves from perditional to traditionalCOLLINS, F. S.Nature genetics. 1995, Vol 9, Num 4, pp 347-350, issn 1061-4036Article

Shattuck lecture : Medical and societal consequences of the human genome projectCOLLINS, F. S.The New England journal of medicine. 1999, Vol 341, Num 1, pp 28-37, issn 0028-4793Article

Cystic fibrosis : molecular biology and therapeutic implicationsCOLLINS, F. S.Science (Washington, D.C.). 1992, Vol 256, Num 5058, pp 774-779, issn 0036-8075Article

Structure of the leukemia-associated human CBFB geneAMITAV HAJRA; COLLINS, F. S.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 571-579, issn 0888-7543Article

Adult turner syndrome associated with chylous ascites and vascular anomaliesTREISMAN, J; COLLINS, F. S.Clinical genetics. 1987, Vol 31, Num 4, pp 218-223, issn 0009-9163Article

pYAC-RC, a yeast artificial chromosome vector for cloning DNA cut with infrequently cutting restriction endonucleasesMARCHUK, D; COLLINS, F. S.Nucleic acids research. 1988, Vol 16, Num 15, issn 0305-1048, 7743Article

The geneticist's approach to complex diseaseSOUMITRA GHOSH; COLLINS, F. S.Annual review of medicine. 1996, Vol 47, pp 333-353, issn 0066-4219Article

The gene for multiple endocrine neoplasia type 1 : Recent findingsMARX, S. J; AGARWAL, S. K; ZHUANG, Z et al.Bone (New York, NY). 1999, Vol 25, Num 1, pp 119-122, issn 8756-3282Conference Paper

New approaches to BRCA1 mutation detectionHACIA, J. G; BRODY, L. C; COLLINS, F. S et al.Breast disease. 1998, Vol 10, Num 1-2, pp 45-59, issn 0888-6008Article

Loss of heterozygosity at llq13: Analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1DONG, Q; DEBELENKO, L. V; COLLINS, F. S et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 5, pp 1416-1420, issn 0021-972XArticle

KVLQT1 mutations in three families with familial or sporadic long QT syndromeRUSSELL, M. W; DICK, M. II; COLLINS, F. S et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1319-1324, issn 0964-6906Article

17q Inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type oneASAMOAH, A; NORTH, K; DORAN, S et al.American journal of medical genetics. 1995, Vol 60, Num 4, pp 312-316, issn 0148-7299Article

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsSTRUEWING, J. P; ABELIOVICH, D; PERETZ, T et al.Nature genetics. 1995, Vol 11, Num 2, pp 198-200, issn 1061-4036Article

Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesisMARLTON, P; CLAXTON, D. F; LIU, P et al.Blood. 1995, Vol 85, Num 3, pp 772-779, issn 0006-4971Article

The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different speciesSAVITSKY, K; SFEZ, S; TAGLE, D. A et al.Human molecular genetics (Print). 1995, Vol 4, Num 11, pp 2025-2032, issn 0964-6906Article

DNA sequences in the promoter region of the NF1 gene are highly conserved between human and mouseHAJRA, A; MARTIN-GALLARDO, A; TARLE, S. A et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 3, pp 649-652, issn 0888-7543Article

Localization of the gene for ATP citrate lyase (ACLY) distal to gastrin (GAS) and proximal to D17S856 on chromosome 17q12-q21COUCH, F. J; ABEL, K. J; BRODY, L. C et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 2, pp 444-446, issn 0888-7543Article

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerCASTILLA, L. H; COUCH, F. J; COLLINS, F. S et al.Nature genetics. 1994, Vol 8, Num 4, pp 387-391, issn 1061-4036Article

An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscleGUTMANN, D. H; ANDERSEN, L. B; COLE, J. L et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, pp 989-992, issn 0964-6906Article

Identification of yeast artificial chromosomes containing the inversion 16 p-arm breakpoint associated with acute myelomonocytic leukemiaPU LIU; CLAXTON, D. F; SICILIANO, M. J et al.Blood. 1993, Vol 82, Num 3, pp 716-721, issn 0006-4971Article

A recombination event that redefines the Huntington disease regionSNELL, R. G; THOMPSON, L. M; HARPER, P. S et al.American journal of human genetics. 1992, Vol 51, Num 2, pp 357-362, issn 0002-9297Article

A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]ANDERSEN, L. B; WALLACE, M. R; MARCHUK, D. A et al.Nucleic acids research. 1991, Vol 19, Num 1, issn 0305-1048, p. 197Article

Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR productsMARCHUK, D; DRUMM, M; SAULINO, A et al.Nucleic acids research. 1991, Vol 19, Num 5, issn 0305-1048, p. 1154Article

A highly polymorphic cDNA probe in the NF1 geneANDERSEN, L. B; WALLACE, M. R; MARCHUK, D. A et al.Nucleic acids research. 1991, Vol 19, Num 13, issn 0305-1048, p. 3754Article

D21S194, a jump clone from D21S16WALKER, A. P; COLLINS, F. S; PATTERSON, D et al.Nucleic acids research. 1990, Vol 18, Num 7, issn 0305-1048, p. 1931Article