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Results: 1-13 |
Results: 13

Authors: WILSON GN
Citation: Gn. Wilson, CORRELATED HEART LIMB ANOMALIES IN MENDELIAN-SYNDROMES PROVIDE EVIDENCE FOR A CARDIOMELIC DEVELOPMENTAL FIELD/, American journal of medical genetics, 76(4), 1998, pp. 297-305

Authors: WILSON GN
Citation: Gn. Wilson, MORE ON SCHOOL-HEALTH AND THE PEDIATRICIAN, Pediatric annals, 27(3), 1998, pp. 118-118

Authors: WILSON KS SCHULTZ RA SCHNEIDER NR WILSON GN EVANS GA
Citation: Ks. Wilson et al., MOLECULAR CYTOGENETIC CHARACTERIZATION OF PARTIAL 11Q TRISOMY IN A CHILD, American journal of human genetics, 61(4), 1997, pp. 815-815

Authors: TONK V SCHULTZ RA CHRISTIAN SL KUBOTA T LEDBETTER DH WILSON GN
Citation: V. Tonk et al., ROBERTSONIAN (15Q-15Q) TRANSLOCATION IN A CHILD WITH ANGELMAN-SYNDROME - EVIDENCE OF UNIPARENTAL DISOMY, American journal of medical genetics, 66(4), 1996, pp. 426-428

Authors: LITTLE BB WILSON GN JACKSON G
Citation: Bb. Little et al., IS THERE A COCAINE SYNDROME - DYSMORPHIC AND ANTHROPOMETRIC ASSESSMENT OF INFANTS EXPOSED TO COCAINE, Teratology, 54(3), 1996, pp. 145-149

Authors: BRYANT DD WILSON GN
Citation: Dd. Bryant et Gn. Wilson, DIFFERENTIAL EVOLUTION AND EXPRESSION OF MURINE PEROXISOMAL MEMBRANE-PROTEIN GENES, Biochemical and molecular medicine, 55(1), 1995, pp. 22-30

Authors: KULHARYA AS MABERRY M KUKOLICH MK DAY DW SCHNEIDER NR WILSON GN TONK V
Citation: As. Kulharya et al., INTERSTITIAL DELETIONS 4Q21.1Q25 AND 4Q25Q27 - PHENOTYPIC VARIABILITYAND RELATION TO RIEGER ANOMALY, American journal of medical genetics, 55(2), 1995, pp. 165-170

Authors: WILSON GN BRYANT DD
Citation: Gn. Wilson et Dd. Bryant, STRUCTURE AND EXPRESSION OF MAMMALIAN PEROXISOME ASSEMBLY FACTOR-I (PMP35) GENES, Biochemical medicine and metabolic biology, 51(2), 1994, pp. 140-148

Authors: WILSON GN
Citation: Gn. Wilson, ATYPICAL INHERITANCE - NEW HORIZONS FOR NEUROLOGY, Neurologic clinics, 12(4), 1994, pp. 663

Authors: WILSON GN
Citation: Gn. Wilson, BASIC BIOMEDICAL-RESEARCH, Science, 266(5189), 1994, pp. 1305-1306

Authors: SCHLICHTEMEIER TL TOMLINSON GE KAMEN BA WABER LJ WILSON GN
Citation: Tl. Schlichtemeier et al., MULTIPLE COAGULATION DEFECTS AND THE COHEN SYNDROME, Clinical genetics, 45(4), 1994, pp. 212-216

Authors: KULHARYA AS SCHNEIDER NR WILSON GN
Citation: As. Kulharya et al., 3 CASES OF DUP(10P) DEL(10Q) SYNDROME RESULTING FROM MATERNAL PERICENTRIC-INVERSION/, American journal of medical genetics, 47(6), 1993, pp. 817-819

Authors: WILSON GN HALL JG DELACRUZ F
Citation: Gn. Wilson et al., GENOMIC IMPRINTING - SUMMARY OF AN NICHHD CONFERENCE, American journal of medical genetics, 46(6), 1993, pp. 675-680
Risultati: 1-13 |