Zoghbi HY - Search Results

1

Balanced X chromosome inactivation patterns in the Rett syndrome brain.

Shahbazian MD, Sun Y, Zoghbi HY. Shahbazian MD, et al. Among authors: zoghbi hy. Am J Med Genet. 2002 Aug 1;111(2):164-8. doi: 10.1002/ajmg.10557. Am J Med Genet. 2002. PMID: 12210344

2

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW. Allen RC, et al. Among authors: zoghbi hy. Am J Hum Genet. 1992 Dec;51(6):1229-39. Am J Hum Genet. 1992. PMID: 1281384 Free PMC article.

3

Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellum.

Eng CM, Durtschi BA, Zoghbi HY, Beaudet AL. Eng CM, et al. Among authors: zoghbi hy. Genomics. 1992 Nov;14(3):813-5. doi: 10.1016/s0888-7543(05)80196-x. Genomics. 1992. PMID: 1294119

4

An easy and rapid method for the detection of chimeric yeast artificial chromosome clones.

Banfi S, Ledbetter SA, Chinault AC, Zoghbi HY. Banfi S, et al. Among authors: zoghbi hy. Nucleic Acids Res. 1992 Apr 11;20(7):1814. doi: 10.1093/nar/20.7.1814. Nucleic Acids Res. 1992. PMID: 1579482 Free PMC article.

5

Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.

Lupski JR, Garcia CA, Zoghbi HY, Hoffman EP, Fenwick RG. Lupski JR, et al. Among authors: zoghbi hy. Am J Med Genet. 1991 Sep 1;40(3):354-64. doi: 10.1002/ajmg.1320400323. Am J Med Genet. 1991. PMID: 1683155

6

Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Ellison KA, Fill CP, Terwilliger J, DeGennaro LJ, Martin-Gallardo A, Anvret M, Percy AK, Ott J, Zoghbi H. Ellison KA, et al. Am J Hum Genet. 1992 Feb;50(2):278-87. Am J Hum Genet. 1992. PMID: 1734712 Free PMC article.

7

Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).

Huang TH, Hejtmancik JF, Edwards A, Pettigrew AL, Herrera CA, Hammond HA, Caskey CT, Zoghbi HY, Ledbetter DH. Huang TH, et al. Among authors: zoghbi hy. Am J Hum Genet. 1991 Dec;49(6):1312-9. Am J Hum Genet. 1991. PMID: 1746558 Free PMC article.

8

Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: analysis of dinucleotide polymorphisms on native gels.

Kwiatkowski TJ Jr, Beaudet AL, Trask BJ, Zoghbi HY. Kwiatkowski TJ Jr, et al. Among authors: zoghbi hy. Genomics. 1991 Aug;10(4):921-6. doi: 10.1016/0888-7543(91)90180-m. Genomics. 1991. PMID: 1916824

9

Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.

Keats BJ, Pollack MS, McCall A, Wilensky MA, Ward LJ, Lu M, Zoghbi HY. Keats BJ, et al. Among authors: zoghbi hy. Am J Hum Genet. 1991 Nov;49(5):972-7. Am J Hum Genet. 1991. PMID: 1928103 Free PMC article.

10

Deletion and linkage mapping of eight markers from the proximal short arm of chromosome 6.

Zoghbi HY, Ballantyne CM, O'Brien WE, McCall AE, Kwiatkowski TJ Jr, Ledbetter SA, Beaudet AL. Zoghbi HY, et al. Genomics. 1990 Feb;6(2):352-7. doi: 10.1016/0888-7543(90)90576-g. Genomics. 1990. PMID: 1968423

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