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Results: 1-7 |
Results: 7
HYPOPIGMENTATION IN THE PRADER-WILLI-SYNDROME CORRELATES WITH P-GENE DELETION BUT NOT WITH HAPLOTYPE OF THE HEMIZYGOTIC P-ALLELE
Authors: SPRITZ RA BAILIN T NICHOLLS RD LEE ST PARK SK MASCARI MJ BUTLER MG
Citation: Ra. Spritz et al., HYPOPIGMENTATION IN THE PRADER-WILLI-SYNDROME CORRELATES WITH P-GENE DELETION BUT NOT WITH HAPLOTYPE OF THE HEMIZYGOTIC P-ALLELE, American journal of medical genetics, 71(1), 1997, pp. 57-62
RELATIONSHIP OF SLEEP ABNORMALITIES TO PATIENT GENOTYPES IN PRADER-WILLI-SYNDROME
Authors: VGONTZAS AN KALES A SEIP J MASCARI MJ BIXLER EO MYERS DC VELABUENO A ROGAN PK
Citation: An. Vgontzas et al., RELATIONSHIP OF SLEEP ABNORMALITIES TO PATIENT GENOTYPES IN PRADER-WILLI-SYNDROME, American journal of medical genetics, 67(5), 1996, pp. 478-482
COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING
Authors: ROGAN PK MASCARI MJ LADDA RL WOODAGE T TRENT RJ SMITH A LAI LW ERICKSON RP CASSIDY SB PETERSEN MB MIKKELSEN M DRISCOLL DJ NICHOLLS RD BUTLER MG
Citation: Pk. Rogan et al., COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING, American journal of medical genetics, 62(3), 1996, pp. 6-6
PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY
Authors: ROGAN PK MASCARI MJ LADDA RL WOODAGE T TRENT RJ SMITH A LAI LW ERICKSON RP CASSIDY SB PETERSEN MB MIKKELSEN M DRISCOLL DJ NICHOLLS RD
Citation: Pk. Rogan et al., PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY, Cytogenetics and cell genetics, 67(1), 1994, pp. 18-18
CONGENITAL CONTRACTURES, ECTODERMAL DYSPLASIA, CLEFT-LIP PALATE, AND DEVELOPMENTAL IMPAIRMENT - A DISTINCT SYNDROME
Authors: LADDA RL ZONANA J RAMER JC MASCARI MJ ROGAN PK
Citation: Rl. Ladda et al., CONGENITAL CONTRACTURES, ECTODERMAL DYSPLASIA, CLEFT-LIP PALATE, AND DEVELOPMENTAL IMPAIRMENT - A DISTINCT SYNDROME, American journal of medical genetics, 47(4), 1993, pp. 550-555
PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY
Authors: MASCARI MJ LADDA RL WOODAGE T TRENT RJ LAI LW ERICKSON RP CASSIDY SB PETERSEN MB MIKKELSEN M DRISCOLL DJ NICHOLLS RD ROGAN PK
Citation: Mj. Mascari et al., PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY, American journal of human genetics, 53(3), 1993, pp. 260-260
UNIPARENTAL DISOMY IN ANGELMAN SYNDROME - A CONSEQUENCE OF PATERNAL MEIOTIC NONDISJUNCTION
Authors: ROGAN PK LICHTY TR LADDA RL MASCARI MJ STEELE MW WENGER SL MALCOLM S DRISCOLL DJ NICHOLLS RD
Citation: Pk. Rogan et al., UNIPARENTAL DISOMY IN ANGELMAN SYNDROME - A CONSEQUENCE OF PATERNAL MEIOTIC NONDISJUNCTION, American journal of human genetics, 53(3), 1993, pp. 1225-1225
Risultati: 1-7 |