Kanis A - Search Results

1

Clinical and genetic characterization of an autosomal dominant nephropathy.

Parvari R, Shnaider A, Basok A, Katchko L, Borochovich Z, Kanis A, Landau D. Parvari R, et al. Among authors: kanis a. Am J Med Genet. 2001 Mar 15;99(3):204-9. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1158>3.0.co;2-p. Am J Med Genet. 2001. PMID: 11241491

2

Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.

Parvari R, Hershkovitz E, Kanis A, Gorodischer R, Shalitin S, Sheffield VC, Carmi R. Parvari R, et al. Among authors: kanis a. Am J Hum Genet. 1998 Jul;63(1):163-9. doi: 10.1086/301915. Am J Hum Genet. 1998. PMID: 9634513 Free PMC article.

3

Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21.

Ghiasvand NM, Kanis AB, Helms C, Sheffield VC, Stone EM, Donis-Keller H. Ghiasvand NM, et al. Among authors: kanis ab. Am J Med Genet. 2000 Jan 17;90(2):165-8. doi: 10.1002/(sici)1096-8628(20000117)90:2<165::aid-ajmg15>3.0.co;2-o. Am J Med Genet. 2000. PMID: 10607958

4

Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci.

Kanis AB, Al-Rajhi AA, Taylor CM, Mathers WD, Folberg RY, Nishimura DY, Sheffield VC, Stone EM. Kanis AB, et al. Ophthalmic Genet. 1999 Dec;20(4):243-9. doi: 10.1076/opge.20.4.243.2273. Ophthalmic Genet. 1999. PMID: 10617922

5

Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling.

Arbour NC, Zlotogora J, Knowlton RG, Merin S, Rosenmann A, Kanis AB, Rokhlina T, Stone EM, Sheffield VC. Arbour NC, et al. Among authors: kanis ab. Hum Mol Genet. 1997 May;6(5):689-94. doi: 10.1093/hmg/6.5.689. Hum Mol Genet. 1997. PMID: 9158143

6

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye.

Nishimura DY, Searby CC, Alward WL, Walton D, Craig JE, Mackey DA, Kawase K, Kanis AB, Patil SR, Stone EM, Sheffield VC. Nishimura DY, et al. Among authors: kanis ab. Am J Hum Genet. 2001 Feb;68(2):364-72. doi: 10.1086/318183. Epub 2001 Jan 18. Am J Hum Genet. 2001. PMID: 11170889 Free PMC article.

7

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25.

Nishimura DY, Swiderski RE, Alward WL, Searby CC, Patil SR, Bennet SR, Kanis AB, Gastier JM, Stone EM, Sheffield VC. Nishimura DY, et al. Among authors: kanis ab. Nat Genet. 1998 Jun;19(2):140-7. doi: 10.1038/493. Nat Genet. 1998. PMID: 9620769

8

Short tandem repeat polymorphic markers for the rat genome from marker-selected libraries.

Walder RY, Garrett MR, McClain AM, Beck GE, Brennan TM, Kramer NA, Kanis AB, Mark AL, Rapp JP, Sheffield VC. Walder RY, et al. Among authors: kanis ab. Mamm Genome. 1998 Dec;9(12):1013-21. doi: 10.1007/s003359900917. Mamm Genome. 1998. PMID: 9880670

9

Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene.

Chatterjee TK, Eapen A, Kanis AB, Fisher RA. Chatterjee TK, et al. Among authors: kanis ab. Genomics. 1997 Oct 15;45(2):429-33. doi: 10.1006/geno.1997.4929. Genomics. 1997. PMID: 9344672

10

Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and partial trisomy 16.

Schmidt N, Van Dyke DC, Keppler-Noreuil K, Muilenburg A, Patil S, Kanis AB. Schmidt N, et al. Among authors: kanis ab. Dev Med Child Neurol. 2001 Feb;43(2):130-2. doi: 10.1017/s0012162201000238. Dev Med Child Neurol. 2001. PMID: 11221902 Free article.

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