Authors:
DESTEFANO AL
CUPPLES LA
ARNOS KS
ASHER JH
BALDWIN CT
BLANTON S
CAREY ML
DASILVA EO
FRIEDMAN TB
GREENBERG J
LALWANI AK
MILUNSKY A
NANCE WE
PANDYA A
RAMESAR RS
READ AP
TASSABEJHI M
WILCOX ER
FARRER LA
Citation: Al. Destefano et al., CORRELATION BETWEEN WAARDENBURG-SYNDROME PHENOTYPE AND GENOTYPE IN A POPULATION OF INDIVIDUALS WITH IDENTIFIED PAX3 MUTATIONS, Human genetics, 102(5), 1998, pp. 499-506
Citation: Ml. Carey et al., SEPTO-OPTIC DYSPLASIA AND WS1 IN THE PROBAND OF A WS1 FAMILY SEGREGATING FOR A NOVEL MUTATION IN PAX3 EXON-7, Journal of Medical Genetics, 35(3), 1998, pp. 248-250
Authors:
SCHMITT ES
PROUD VK
BOYD EF
SPINNER RJ
CAREY ML
SCHWARTZ CF
FRIEDMAN TB
Citation: Es. Schmitt et al., CLINICAL AND MOLECULAR STUDIES OF PAX3 AND TWIST MUTATIONS IN A UNIQUE 5-GENERATION FAMILY WITH CRANIOFACIAL MALFORMATIONS, HETEROCHROMIA, AND WHITE HAIR PATCHES, American journal of human genetics, 61(4), 1997, pp. 628-628
Authors:
MORELL R
CAREY ML
LALWANI AK
FRIEDMAN TB
ASHER JH
Citation: R. Morell et al., 3 MUTATIONS IN THE PAIRED HOMEODOMAIN OF PAX3 THAT CAUSE WAARDENBURG SYNDROME TYPE-1, Human heredity, 47(1), 1997, pp. 38-41
Authors:
ASHER JH
HARRISON RW
MORELL R
CAREY ML
FRIEDMAN TB
Citation: Jh. Asher et al., EFFECTS OF PAX3 MODIFIER GENES ON CRANIOFACIAL MORPHOLOGY, PIGMENTATION, AND VIABILITY - A MURINE MODEL OF WAARDENBURG SYNDROME VARIATION, Genomics, 34(3), 1996, pp. 285-298