Gu H - Search Results

1

Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.

Jenkins EC, Genovese MJ, Duncan CJ, Gu H, Stark-Houck SL, Lele K, Li SY, Krawczun MS. Jenkins EC, et al. Among authors: gu h. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):136-41. doi: 10.1002/ajmg.1320430121. Am J Med Genet. 1992. PMID: 1605182

2

Dialyzed fetal bovine serum increases cytogenetic fragile X expression.

Jenkins EC, Duncan CJ, Gu H, Genovese M, Krawczun MS. Jenkins EC, et al. Among authors: gu h. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):155-60. doi: 10.1002/ajmg.1320430124. Am J Med Genet. 1992. PMID: 1534967

3

Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures.

Jenkins EC, Krawczun MS, Stark-Houck SL, Duncan CJ, Kunaporn S, Gu H, Schwartz-Richstein C, Howard-Peebles PN, Gross A, Sherman SL, et al. Jenkins EC, et al. Among authors: gu h. Am J Med Genet. 1991 Feb-Mar;38(2-3):447-52. doi: 10.1002/ajmg.1320380262. Am J Med Genet. 1991. PMID: 1826813

4

Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis.

Krawczun MS, Jenkins EC, Duncan CJ, Stark-Houck SL, Kunaporn S, Schwatz-Richstein C, Gu H, Brown WT. Krawczun MS, et al. Among authors: gu h. Am J Med Genet. 1991 Feb-Mar;38(2-3):456-63. doi: 10.1002/ajmg.1320380264. Am J Med Genet. 1991. PMID: 2018087

5

Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures.

Jenkins EC, Duncan CJ, Sanz MM, Genovese M, Gu H, Schwartz-Richstein C, Lele KP, Salandi ML, Krawczun MS. Jenkins EC, et al. Among authors: gu h. Pathobiology. 1990;58(4):236-40. doi: 10.1159/000163591. Pathobiology. 1990. PMID: 2147548

6

Normal adaptive function with learning disability in duplication 8p including band p22.

Sklower Brooks SS, Genovese M, Gu H, Duncan CJ, Shanske A, Jenkins EC. Sklower Brooks SS, et al. Among authors: gu h. Am J Med Genet. 1998 Jun 30;78(2):114-7. doi: 10.1002/(sici)1096-8628(19980630)78:2<114::aid-ajmg3>3.3.co;2-6. Am J Med Genet. 1998. PMID: 9674899

7

Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene.

Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Jenkins EC, et al. Among authors: gu h. Am J Med Genet A. 2008 Jun 15;146A(12):1543-6. doi: 10.1002/ajmg.a.32342. Am J Med Genet A. 2008. PMID: 18478592 Free PMC article.

8

Occurrence of aneuploidy for the X chromosome in over 1,300 unrelated specimens screened for the fragile X chromosome.

Jenkins EC, Genovese M, Duncan CJ, Gu H, Stark-Houck S, Li SY, Henderson J, Morys I, Brown WT. Jenkins EC, et al. Among authors: gu h. Am J Med Genet. 1994 Jul 15;51(4):452-3. doi: 10.1002/ajmg.1320510430. Am J Med Genet. 1994. PMID: 7943017 No abstract available.

9

The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.

Velinov M, Gu H, Genovese M, Duncan C, Brown WT, Jenkins E. Velinov M, et al. Among authors: gu h. Mol Genet Metab. 2000 Jan;69(1):81-3. doi: 10.1006/mgme.1999.2941. Mol Genet Metab. 2000. PMID: 10655162

10

Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.

Velinov M, Gu H, Genovese M, Duncan C, Warburton P, Brooks SS, Jenkins EC. Velinov M, et al. Among authors: gu h. Ann Genet. 2004 Apr-Jun;47(2):199-205. doi: 10.1016/j.anngen.2004.02.005. Ann Genet. 2004. PMID: 15183754

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