Asher JH Jr - Search Results

1

Auditory brainstem responses in Golden Syrian hamsters (Mesocricetus auratus) affected with the Wh gene.

Amedofu GK, Gopal KV, Asher JH Jr, Ahmadizadeh M, Moore EJ. Amedofu GK, et al. Among authors: asher jh jr. Lab Anim Sci. 1999 Apr;49(2):173-8. Lab Anim Sci. 1999. PMID: 10331547

2

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.

DeStefano AL, Cupples LA, Arnos KS, Asher JH Jr, Baldwin CT, Blanton S, Carey ML, da Silva EO, Friedman TB, Greenberg J, Lalwani AK, Milunsky A, Nance WE, Pandya A, Ramesar RS, Read AP, Tassabejhi M, Wilcox ER, Farrer LA. DeStefano AL, et al. Among authors: asher jh jr. Hum Genet. 1998 May;102(5):499-506. doi: 10.1007/s004390050732. Hum Genet. 1998. PMID: 9654197

3

Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2.

Hodgkinson CA, Nakayama A, Li H, Swenson LB, Opdecamp K, Asher JH Jr, Arnheiter H, Glaser T. Hodgkinson CA, et al. Among authors: asher jh jr. Hum Mol Genet. 1998 Apr;7(4):703-8. doi: 10.1093/hmg/7.4.703. Hum Mol Genet. 1998. PMID: 9499424

4

Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7.

Carey ML, Friedman TB, Asher JH Jr, Innis JW. Carey ML, et al. Among authors: asher jh jr. J Med Genet. 1998 Mar;35(3):248-50. doi: 10.1136/jmg.35.3.248. J Med Genet. 1998. PMID: 9541113 Free PMC article.

5

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.

Innis JW, Asher JH Jr, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB. Innis JW, et al. Among authors: asher jh jr. Am J Med Genet. 1997 Aug 22;71(3):292-7. Am J Med Genet. 1997. PMID: 9268099 Free article.

6

Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies.

Innis JW, Asher JH Jr, Poznanski AK, Sheldon S. Innis JW, et al. Among authors: asher jh jr. Am J Med Genet. 1997 Aug 8;71(2):150-5. doi: 10.1002/(sici)1096-8628(19970808)71:2<150::aid-ajmg6>3.0.co;2-1. Am J Med Genet. 1997. PMID: 9217213 Free article.

7

The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1).

Morell R, Friedman TB, Asher JH Jr, Robbins LG. Morell R, et al. Among authors: asher jh jr. J Med Genet. 1997 Jun;34(6):447-52. doi: 10.1136/jmg.34.6.447. J Med Genet. 1997. PMID: 9192262 Free PMC article. Review.

8

Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA).

Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH Jr. Morell R, et al. Among authors: asher jh jr. Hum Mol Genet. 1997 May;6(5):659-64. doi: 10.1093/hmg/6.5.659. Hum Mol Genet. 1997. PMID: 9158138

9

Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter.

Liang Y, Chen H, Asher JH Jr, Chang CC, Friedman TB. Liang Y, et al. Among authors: asher jh jr. Gene. 1997 Jan 15;184(2):163-7. doi: 10.1016/s0378-1119(96)00590-2. Gene. 1997. PMID: 9031623

10

Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1.

Morell R, Carey ML, Lalwani AK, Friedman TB, Asher JH Jr. Morell R, et al. Among authors: asher jh jr. Hum Hered. 1997 Jan-Feb;47(1):38-41. doi: 10.1159/000154387. Hum Hered. 1997. PMID: 9017978

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