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Refined genetic mapping of X-linked thoracoabdominal syndrome.
Parvari R, Carmi R, Weissenbach J, Pilia G, Mumm S, Weinstein Y. Parvari R, et al. Among authors: weissenbach j. Am J Med Genet. 1996 Feb 2;61(4):401-2. doi: 10.1002/(SICI)1096-8628(19960202)61:4<401::AID-AJMG18>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8834056 No abstract available.
Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.
Froggatt NJ, Koch J, Davies R, Evans DG, Clamp A, Quarrell OW, Weissenbach J, Hodgson SV, Ponder BA, Barton DE, et al. Froggatt NJ, et al. Among authors: weissenbach j. J Med Genet. 1995 May;32(5):352-7. doi: 10.1136/jmg.32.5.352. J Med Genet. 1995. PMID: 7616541 Free PMC article.
No evidence of genetic heterogeneity in dominant optic atrophy.
Bonneau D, Souied E, Gerber S, Rozet JM, D'Haens E, Journel H, Plessis G, Weissenbach J, Munnich A, Kaplan J. Bonneau D, et al. Among authors: weissenbach j. J Med Genet. 1995 Dec;32(12):951-3. doi: 10.1136/jmg.32.12.951. J Med Genet. 1995. PMID: 8825922 Free PMC article.
Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1.
Carrié A, Nepotes V, Billuart P, Beldjord C, Bienvenu T, Chelly J, Bruls T, Heilig R, Weissenbach J, Jun L, Marynen P. Carrié A, et al. Among authors: weissenbach j. Am J Med Genet. 1999 Jul 30;85(3):252-4. doi: 10.1002/(sici)1096-8628(19990730)85:3<252::aid-ajmg13>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10398238 No abstract available.
Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q.
van Herwerden L, Rose CS, Reardon W, Brueton LA, Weissenbach J, Malcolm S, Winter RM. van Herwerden L, et al. Among authors: weissenbach j. Am J Hum Genet. 1994 Apr;54(4):669-74. Am J Hum Genet. 1994. PMID: 8128964 Free PMC article.
505 results