Kaplan J - Search Results

1

Structure and refinement of the physical mapping of the gamma- glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma.

Rozet JM, Gerber S, Perrault I, Calvas P, Souied E, Châtelin S, Viegas-Péquignot, Molina-Gomez D, Munnich A, Kaplan J. Rozet JM, et al. Among authors: kaplan j. Cytogenet Cell Genet. 1998;82(1-2):91-4. doi: 10.1159/000015072. Cytogenet Cell Genet. 1998. PMID: 9841137

2

Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease.

Gerber S, Rozet JM, Bonneau D, Souied E, Weissenbach J, Frezal J, Munnich A, Kaplan J. Gerber S, et al. Among authors: kaplan j. Hum Genet. 1995 Apr;95(4):382-4. doi: 10.1007/BF00208959. Hum Genet. 1995. PMID: 7705831

3

A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.

Gerber S, Rozet JM, Bonneau D, Souied E, Camuzat A, Dufier JL, Amalric P, Weissenbach J, Munnich A, Kaplan J. Gerber S, et al. Among authors: kaplan j. Am J Hum Genet. 1995 Feb;56(2):396-9. Am J Hum Genet. 1995. PMID: 7847373 Free PMC article.

4

Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13.

Camuzat A, Rozet JM, Dollfus H, Gerber S, Perrault I, Weissenbach J, Munnich A, Kaplan J. Camuzat A, et al. Among authors: kaplan j. Hum Genet. 1996 Jun;97(6):798-801. doi: 10.1007/BF02346192. Hum Genet. 1996. PMID: 8641699

5

Structure and physical mapping of DR1, a TATA-binding protein-associated phosphoprotein gene, to chromosome 1p22.1 and its exclusion in Stargardt disease (STGD).

Rozet JM, Gerber S, Perrault I, Camuzat A, Calvas P, Viegas-Pequignot E, Molina-Gomes D, Le Paslier D, Chumakov I, Munnich A, Kaplan J. Rozet JM, et al. Among authors: kaplan j. Genomics. 1996 Sep 15;36(3):554-6. doi: 10.1006/geno.1996.0508. Genomics. 1996. PMID: 8884286 No abstract available.

6

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3.

Cabot A, Rozet JM, Gerber S, Perrault I, Ducroq D, Smahi A, Souied E, Munnich A, Kaplan J. Cabot A, et al. Among authors: kaplan j. Am J Hum Genet. 1999 Apr;64(4):1141-6. doi: 10.1086/302324. Am J Hum Genet. 1999. PMID: 10090899 Free PMC article.

7

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus.

Rozet JM, Gerber S, Ghazi I, Perrault I, Ducroq D, Souied E, Cabot A, Dufier JL, Munnich A, Kaplan J. Rozet JM, et al. Among authors: kaplan j. J Med Genet. 1999 Jun;36(6):447-51. J Med Genet. 1999. PMID: 10874631 Free PMC article.

8

A gene for Usher syndrome type I (USH1A) maps to chromosome 14q.

Kaplan J, Gerber S, Bonneau D, Rozet JM, Delrieu O, Briard ML, Dollfus H, Ghazi I, Dufier JL, Frézal J, et al. Kaplan J, et al. Genomics. 1992 Dec;14(4):979-87. doi: 10.1016/s0888-7543(05)80120-x. Genomics. 1992. PMID: 1478676

9

DsaI polymorphism at the human cone transducin alpha-subunit (GNAT2) detected by PCR.

Rozet JM, Gerber S, Bonneau D, Munnich A, Kaplan J. Rozet JM, et al. Among authors: kaplan j. Hum Mol Genet. 1994 Jun;3(6):1030. doi: 10.1093/hmg/3.6.1030-a. Hum Mol Genet. 1994. PMID: 7951223 No abstract available.

10

Dinucleotide repeat polymorphism at the human protein C inhibitor (PCI) locus.

Larget-Piet D, Rozet JM, Gerber S, Dollfus H, Munnich A, Kaplan J. Larget-Piet D, et al. Among authors: kaplan j. Hum Mol Genet. 1993 Dec;2(12):2201. doi: 10.1093/hmg/2.12.2201-a. Hum Mol Genet. 1993. PMID: 8111401 No abstract available.

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