Gu H - Search Results

1

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

2

PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensions.

Velinov M, Gu H, Shah K, Genovese M, Duncan C, Kupchik G, Jenkins EC. Velinov M, et al. Among authors: gu h. Genet Test. 2001 Summer;5(2):153-5. doi: 10.1089/109065701753145655. Genet Test. 2001. PMID: 11551105

3

Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation.

Velinov M, Gu H, Yeboa K, Warburton D, Tubo T, Dhuper S, Lanter S, Delprino D, Kupchik G, Jenkins EC. Velinov M, et al. Among authors: gu h. Am J Med Genet. 2002 Feb 1;107(4):330-3. doi: 10.1002/ajmg.10140. Am J Med Genet. 2002. PMID: 11840491

4

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

5

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

6

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

7

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

8

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

9

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

10

Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.

Velinov M, Kupferman J, Gu H, Macera MJ, Babu A, Jenkins EC, Kupchik G. Velinov M, et al. Among authors: gu h. Eur J Med Genet. 2005 Jan-Mar;48(1):51-5. doi: 10.1016/j.ejmg.2005.01.008. Epub 2005 Feb 12. Eur J Med Genet. 2005. PMID: 15953406

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