J. H. Asher

发表

Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

K. Arnos, L. Farrer, C. Baldwin, 1994, American journal of human genetics.

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

K. Arnos, L. Farrer, P. Beighton, 1992, American journal of human genetics.

Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.

T. Friedman, R. Morell, J. H. Asher, 1991, American journal of human genetics.

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

G. Amedofu, K. Gopal, E. J. Moore, 1999, Laboratory animal science.

The Genetic Structure and Evolutionary Fate of Parthenogenetic Amphibian Populations as Determined by Markovian Analysis

J. H. Asher, G. W. Nace, 1971 .

A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1.

T. Barber, T. Friedman, R. Morell, 1993, Human molecular genetics.

Missense mutation in the paired domain of PAX3 causes craniofacial‐deafness‐hand syndrome

T. Friedman, R. Morell, J. H. Asher, 1996, Human mutation.

Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variation.

T. Friedman, R. Morell, J. H. Asher, 1996, Genomics.

Parthenogenesis and genetic variability. I. Linkage and inbreeding estimations in the frog, Rana pipiens.

G. Nace, J. H. Asher, C. Richards, 1970, Genetics.

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

R. Spritz, T. Friedman, J. Pierpont, 1997, Human molecular genetics.

Mouse and hamster mutants as models for Waardenburg syndromes in humans.

T. Friedman, J. H. Asher, 1990, Journal of medical genetics.

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

T. Friedman, L. G. Robbins, R. Morell, 1997, Journal of medical genetics.

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

H. Li, T. Glaser, C. Hodgkinson, 1998, Human molecular genetics.

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

T. Friedman, J. Innis, J. H. Asher, 1998, Journal of medical genetics.

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17

J. Weber, T. Barber, T. Friedman, 1995, Nature Genetics.

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family.

T. Friedman, R. Morell, S. Moeljopawiro, 1992, Human molecular genetics.

ONE-LOCUS MODELS FOR VARIOUS DIPLOID POPULATIONS 1 *

J. H. Asher, 2003 .

Effects of pinealectomy on reproduction in the Syrian hamster mutant anophthalmic white (Wh).

J. H. Asher, S. Hagen, 1983, The American journal of anatomy.

Parthenogenesis and genetic variability. II. One-locus models for various diploid populations.

J. H. Asher, 1970, Genetics.

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.

T. Friedman, T. Glover, J. Innis, 1997, American journal of medical genetics.

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

K. Arnos, A. Pandya, L. Farrer, 1998, Human Genetics.

Concerning the primary defect leading to the pleiotropic effects caused by anophthalmic white (Wh) in the Syrian hamster Mesocricetus auratus.

J. H. Asher, 1981, The Journal of experimental zoology.

A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) family.

T. Friedman, R. Morell, J. H. Asher, 1993, Human molecular genetics.

A comparison of some serological and biological properties of seven isolates of tobacco ringspot virus.

R. Gergerich, D. Ramsdell, J. H. Asher, 1983 .

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.

T. Friedman, C. Chang, J. H. Asher, 1997, Gene.

Confirmation of the Location of a Waardenburg Syndrome Type I Mutation on Human Chromosome 2q a

R. Morell, Thomas B. Friedman, J. H. Asher, 1991 .

Effects of the gene Wh on reproduction in the Syrian hamster, Mesocricetus auratus.

G. Hooper, J. H. Asher, S. James, 1980, The Journal of experimental zoology.

Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.

S. Moeljopawiro, S. Winata, J. H. Asher, 1995, Journal of medical genetics.