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Results: 1-7 |
Results: 7
TENASCIN-X DEFICIENCY IS ASSOCIATED WITH EHLERS-DANLOS-SYNDROME
Authors: BURCH GH GONG Y LIU WH DETTMAN RW CURRY CJ SMITH L MILLER WL BRISTOW J
Citation: Gh. Burch et al., TENASCIN-X DEFICIENCY IS ASSOCIATED WITH EHLERS-DANLOS-SYNDROME, Nature genetics, 17(1), 1997, pp. 104-108
EVALUATION OF MENTAL-RETARDATION - RECOMMENDATIONS OF A CONSENSUS CONFERENCE
Authors: CURRY CJ STEVENSON RE AUGHTON D BYRNE J CAREY JC CASSIDY S CUNNIFF C GRAHAM JM JONES MC KABACK MM MOESCHLER J SCHAEFER GB SCHWARTZ S TARLETON J OPITZ J
Citation: Cj. Curry et al., EVALUATION OF MENTAL-RETARDATION - RECOMMENDATIONS OF A CONSENSUS CONFERENCE, American journal of medical genetics, 72(4), 1997, pp. 468-477
RITSCHER-SCHINZEL (3C) SYNDROME - DOCUMENTATION OF THE PHENOTYPE
Authors: KOSAKI K CURRY CJ ROEDER E JONES KL
Citation: K. Kosaki et al., RITSCHER-SCHINZEL (3C) SYNDROME - DOCUMENTATION OF THE PHENOTYPE, American journal of medical genetics, 68(4), 1997, pp. 421-427
NEONATAL HEMOCHROMATOSIS
Authors: CURRY CJ SCHORNHORST D FISHER J MONDOZA J WINTER S KNISELY A
Citation: Cj. Curry et al., NEONATAL HEMOCHROMATOSIS, American journal of human genetics, 61(4), 1997, pp. 529-529
ATELOSTEOGENESIS TYPE-I - LACK OF EVIDENCE FOR A SULFATE TRANSPORT DISORDER
Authors: HASTRUP W DELOZIERBLANCHET CD SCHARNHORST D SUPERTIFURGA A CURRY CJ
Citation: W. Hastrup et al., ATELOSTEOGENESIS TYPE-I - LACK OF EVIDENCE FOR A SULFATE TRANSPORT DISORDER, American journal of human genetics, 61(4), 1997, pp. 560-560
DIAGNOSTIC YIELD OF GENETIC EVALUATIONS IN DEVELOPMENTAL DELAY MENTAL-RETARDATION
Authors: CURRY CJ SANDHU A FRUTOS L WELLS R
Citation: Cj. Curry et al., DIAGNOSTIC YIELD OF GENETIC EVALUATIONS IN DEVELOPMENTAL DELAY MENTAL-RETARDATION, Journal of investigative medicine, 44(1), 1996, pp. 130-130
NEUROFIBROMATOSIS-NOONAN SYNDROME
Authors: BUEHNING L CURRY CJ
Citation: L. Buehning et Cj. Curry, NEUROFIBROMATOSIS-NOONAN SYNDROME, Pediatric dermatology, 12(3), 1995, pp. 267-271
Risultati: 1-7 |