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Results: 1-6 |
Results: 6

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

Authors: CAREY ML FRIEDMAN TB ASHER JH INNIS JW
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

Authors: CAREY ML LIANG Y BARBER TD MORELL R JOHNSON DH COX S ASHER JH FRIEDMAN TB
Citation: Ml. Carey et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT D14S542, Human molecular genetics, 3(9), 1994, pp. 1712-1712
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