Zoghbi HY - Search Results

1

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.

Ferrero GB, Franco B, Roth EJ, Firulli BA, Borsani G, Delmas-Mata J, Weissenbach J, Halley G, Schlessinger D, Chinault AC, Zoghbi HY, Nelson DL, Ballabio A. Ferrero GB, et al. Among authors: zoghbi hy. Hum Mol Genet. 1995 Oct;4(10):1821-7. doi: 10.1093/hmg/4.10.1821. Hum Mol Genet. 1995. PMID: 8595402

2

A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.

Wapenaar MC, Schiaffino MV, Bassi MT, Schaefer L, Chinault AC, Zoghbi HY, Ballabio A. Wapenaar MC, et al. Among authors: zoghbi hy. Hum Mol Genet. 1994 Jul;3(7):1155-61. doi: 10.1093/hmg/3.7.1155. Hum Mol Genet. 1994. PMID: 7981686

3

A gene from the Xp22.3 region shares homology with voltage-gated chloride channels.

van Slegtenhorst MA, Bassi MT, Borsani G, Wapenaar MC, Ferrero GB, de Conciliis L, Rugarli EI, Grillo A, Franco B, Zoghbi HY, Ballabio A. van Slegtenhorst MA, et al. Among authors: zoghbi hy. Hum Mol Genet. 1994 Apr;3(4):547-52. doi: 10.1093/hmg/3.4.547. Hum Mol Genet. 1994. PMID: 8069296

4

Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.

Ellison KA, Roth EJ, McCabe ER, Chinault AC, Zoghbi HY. Ellison KA, et al. Among authors: zoghbi hy. Am J Med Genet. 1993 Nov 15;47(7):1124-34. doi: 10.1002/ajmg.1320470736. Am J Med Genet. 1993. PMID: 8291533

5

Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.

Banfi S, Chung MY, Kwiatkowski TJ Jr, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY. Banfi S, et al. Among authors: zoghbi hy. Genomics. 1993 Dec;18(3):627-35. doi: 10.1016/s0888-7543(05)80365-9. Genomics. 1993. PMID: 8307572

6

A high resolution deletion map of human chromosome Xp22.

Schaefer L, Ferrero GB, Grillo A, Bassi MT, Roth EJ, Wapenaar MC, van Ommen GJ, Mohandas TK, Rocchi M, Zoghbi HY, Ballabio A. Schaefer L, et al. Among authors: zoghbi hy. Nat Genet. 1993 Jul;4(3):272-9. doi: 10.1038/ng0793-272. Nat Genet. 1993. PMID: 8358436

7

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions.

Wapenaar MC, Bassi MT, Schaefer L, Grillo A, Ferrero GB, Chinault AC, Ballabio A, Zoghbi HY. Wapenaar MC, et al. Among authors: zoghbi hy. Hum Mol Genet. 1993 Jul;2(7):947-52. doi: 10.1093/hmg/2.7.947. Hum Mol Genet. 1993. PMID: 8364577

8

Rapid identification of yeast artificial chromosome clones by matrix pooling and crude lysate PCR.

Kwiatkowski TJ Jr, Zoghbi HY, Ledbetter SA, Ellison KA, Chinault AC. Kwiatkowski TJ Jr, et al. Among authors: zoghbi hy. Nucleic Acids Res. 1990 Dec 11;18(23):7191-2. doi: 10.1093/nar/18.23.7191. Nucleic Acids Res. 1990. PMID: 2263507 Free PMC article.

9

Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

Lindsay EA, Grillo A, Ferrero GB, Roth EJ, Magenis E, Grompe M, Hultén M, Gould C, Baldini A, Zoghbi HY, et al. Lindsay EA, et al. Among authors: zoghbi hy. Am J Med Genet. 1994 Jan 15;49(2):229-34. doi: 10.1002/ajmg.1320490214. Am J Med Genet. 1994. PMID: 8116674

10

Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS).

Schaefer L, Ballabio A, Zoghbi HY. Schaefer L, et al. Among authors: zoghbi hy. Genomics. 1996 Jun 1;34(2):166-72. doi: 10.1006/geno.1996.0261. Genomics. 1996. PMID: 8661044

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