Lynch ED - Search Results

1

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.

Lebo RV, Chance PF, Dyck PJ, Redila-Flores MT, Lynch ED, Golbus MS, Bird TD, King MC, Anderson LA, Hall J, et al. Lebo RV, et al. Among authors: lynch ed. Hum Genet. 1991 Nov;88(1):1-12. doi: 10.1007/BF00204921. Hum Genet. 1991. PMID: 1683643

2

Prenatal diagnosis with repetitive in situ hybridization probes.

Lebo RV, Flandermeyer RR, Diukman R, Lynch ED, Lepercq JA, Golbus MS. Lebo RV, et al. Among authors: lynch ed. Am J Med Genet. 1992 Jul 15;43(5):848-54. doi: 10.1002/ajmg.1320430519. Am J Med Genet. 1992. PMID: 1642274

3

Multicolor fluorescence in situ hybridization and pulsed field electrophoresis dissect CMT1B gene region.

Lebo RV, Lynch ED, Wiegant J, Moore K, Trounstine M, van der Ploeg M. Lebo RV, et al. Among authors: lynch ed. Hum Genet. 1991 Nov;88(1):13-20. doi: 10.1007/BF00204922. Hum Genet. 1991. PMID: 1683644

4

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers.

Lebo RV, Lynch ED, Bird TD, Golbus MS, Barker DF, O'Connell P, Chance PF. Lebo RV, et al. Among authors: lynch ed. Am J Hum Genet. 1992 Jan;50(1):42-55. Am J Hum Genet. 1992. PMID: 1729894 Free PMC article.

5

Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence.

Lebo RV, Anderson LA, DiMauro S, Lynch E, Hwang P, Fletterick R. Lebo RV, et al. Hum Genet. 1990 Nov;86(1):17-24. doi: 10.1007/BF00205166. Hum Genet. 1990. PMID: 1701414

6

Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridization.

Lebo RV, Martelli L, Su Y, Li L, Lynch E, Mansfield E, Pua KH, Watson DF, Chueh J, Hurko O. Lebo RV, et al. Am J Med Genet. 1993 Sep 1;47(3):441-50. doi: 10.1002/ajmg.1320470334. Am J Med Genet. 1993. PMID: 8135298

7

Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization.

Bonifas JM, Bare JW, Lynch ED, Lebo RV, Epstein EH Jr. Bonifas JM, et al. Among authors: lynch ed. Genomics. 1992 Jun;13(2):452-4. doi: 10.1016/0888-7543(92)90270-3. Genomics. 1992. PMID: 1377166

8

Prenatal in situ hybridization test for deleted steroid sulfatase gene.

Lebo RV, Lynch ED, Golbus MS, Flandermeyer RR, Yen PH, Shapiro LJ. Lebo RV, et al. Among authors: lynch ed. Am J Med Genet. 1993 Jul 1;46(6):652-8. doi: 10.1002/ajmg.1320460610. Am J Med Genet. 1993. PMID: 8362907

9

Two independent polymorphisms at the 17 beta-hydroxysteroid dehydrogenase (EDH17B) gene (17q21).

Friedman LS, Lynch ED, King MC. Friedman LS, et al. Among authors: lynch ed. Hum Mol Genet. 1993 Jun;2(6):821. doi: 10.1093/hmg/2.6.821. Hum Mol Genet. 1993. PMID: 8394763 No abstract available.

10

High-density genetic map of the BRCA1 region of chromosome 17q12-q21.

Anderson LA, Friedman L, Osborne-Lawrence S, Lynch E, Weissenbach J, Bowcock A, King MC. Anderson LA, et al. Genomics. 1993 Sep;17(3):618-23. doi: 10.1006/geno.1993.1381. Genomics. 1993. PMID: 8244378

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