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Results: 1-25/39
Authors:
ROGAN PK
SEIP JR
KNOLL JHM
WHITE LM
WENGER SL
STEELE MW
SPERLING MA
APARICIO L
MENON R
Citation: Pk. Rogan et al., RELAXATION OF IMPRINTING IN PATIENTS WITH PRADER-WILLI-SYNDROME, American journal of medical genetics, 73(4), 1997, pp. 2-2
Authors:
WENGER SL
SELL SL
PAINTER MJ
STEELE MW
Citation: Sl. Wenger et al., INHERITED UNBALANCED SUBTELOMERIC TRANSLOCATION IN A CHILD WITH 8P-SYNDROME AND ANGELMAN-SYNDROME, American journal of medical genetics, 70(2), 1997, pp. 150-154
Authors:
RUBINSTEIN WS
WENGER SL
HOFFMAN RM
AUERBACH AD
MULVIHILL JJ
Citation: Ws. Rubinstein et al., INTERSTITIAL LUNG-DISEASE IN AN ADULT WITH FANCONI-ANEMIA - CLUES TO THE PATHOGENESIS, American journal of medical genetics, 69(3), 1997, pp. 315-319
Authors:
WENGER SL
MCPHERSON EW
Citation: Sl. Wenger et Ew. Mcpherson, INTERSTITIAL DELETION 2(P11.2P13) - A RARE CHROMOSOMAL ABNORMALITY, Clinical genetics, 52(1), 1997, pp. 61-62
Authors:
WENGER SL
BOONE LY
SURTI U
STEELE MW
Citation: Sl. Wenger et al., TERMINAL 2Q DELETION - A RECOGNIZABLE SYNDROME, Clinical genetics, 51(4), 1997, pp. 290-290
Authors:
BANKE MG
WENGER SL
CUMMINS JH
BAY CA
Citation: Mg. Banke et al., CHROMOSOMAL ORIGIN, FREQUENCIES, AND PHENOTYPIC CORRELATIONS OF MARKER CHROMOSOMES - 5 CASES AND A REVIEW OF THE LITERATURE, American journal of human genetics, 61(4), 1997, pp. 668-668
Authors:
CUTENESE CL
HUMMEL M
MULLETT MD
WENGER SL
Citation: Cl. Cutenese et al., RING CHROMOSOME-1 IN NEWBORN, American journal of human genetics, 61(4), 1997, pp. 686-686
Authors:
WENGER SL
SELL SL
LENKEY SG
CUMMINS JH
FRIDAY GA
CARTNER JC
BAY CA
Citation: Sl. Wenger et al., MARKER CHROMOSOME IN POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE-I (PAS) RELATED TO DISEASE PROCESS, American journal of human genetics, 61(4), 1997, pp. 813-813
Authors:
MANKSEYMOUR AR
CUMMINS JH
WENGER SL
BAY CA
Citation: Ar. Mankseymour et al., TERMINAL TRANSVERSE LIMB DEFECT IN A PATIENT WITH VELO-CARDIO-FACIAL SYNDROME (VCFS) AND THE 22Q11.2 DELETION, American journal of human genetics, 61(4), 1997, pp. 2162-2162
Authors:
OLINSKY S
LOOP BT
DEKOSKY A
RIPEPI B
WENG W
CUMMINS J
WENGER SL
YAN Y
LAGENAUR C
NARAYANAN V
Citation: S. Olinsky et al., CHROMOSOMAL MAPPING OF THE HUMAN M6 GENES, Genomics, 33(3), 1996, pp. 532-536
Authors:
GREALLY JM
NEISWANGER K
CUMMINS JH
BOONE LY
LENKEY SG
WENGER SL
LEWIS JL
FISCHER D
PAUL RA
STEELE MW
Citation: Jm. Greally et al., A MOLECULAR ANATOMICAL ANALYSIS OF MOSAIC TRISOMY-16, Human genetics, 98(1), 1996, pp. 86-90
Authors:
WENGER SL
SELL SL
PAINTER MJ
STEELE MW
Citation: Sl. Wenger et al., IS IT ANGELMAN SYNDROME - A CHILD WITH A 45,XY,-8,-15,-15)(P23.3-Q13)KARYOTYPE(DER(8)T(8), Cytogenetics and cell genetics, 74(4), 1996, pp. 303-304
Authors:
MOONEY MP
ASTON CE
SIEGEL MI
LOSKEN HW
SMITH TD
BURROWS AM
WENGER SL
CARUSO K
SIEGEL B
FERRELL RE
Citation: Mp. Mooney et al., CRANIOSYNOSTOSIS WITH AUTOSOMAL-DOMINANT TRANSMISSION IN NEW-ZEALAND WHITE-RABBITS, Journal of craniofacial genetics and developmental biology, 16(1), 1996, pp. 52-63
Authors:
WENGER SL
GIANGRECO CA
TARLETON J
WESSEL HB
Citation: Sl. Wenger et al., INABILITY TO INDUCE FRAGILE SITES AT CTG REPEATS IN CONGENITAL MYOTONIC-DYSTROPHY, American journal of medical genetics, 66(1), 1996, pp. 60-63
Authors:
GIANGRECO CA
STEELE MW
ASTON CE
CUMMINS JH
WENGER SL
Citation: Ca. Giangreco et al., A SIMPLIFIED 6-ITEM CHECKLIST FOR SCREENING FOR FRAGILE-X SYNDROME INTHE PEDIATRIC POPULATION, The Journal of pediatrics, 129(4), 1996, pp. 611-614
Authors:
WENGER SL
CUMMINS JH
Citation: Sl. Wenger et Jh. Cummins, FLUORESCENT IN-SITU HYBRIDIZATION FOR DIAGNOSIS OF PRADER-WILLI ANGELMAN SYNDROME, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 115-115
Authors:
WENGER SL
Citation: Sl. Wenger, CHEMICAL INDUCTION OF SISTER-CHROMATID EXCHANGE AT FRAGILE SITES, Cancer genetics and cytogenetics, 85(1), 1995, pp. 72-74
Authors:
LEWIS KE
LUBETSKY MJ
WENGER SL
STEELE MW
Citation: Ke. Lewis et al., CHROMOSOMAL-ABNORMALITIES IN A PSYCHIATRIC POPULATION, American journal of medical genetics, 60(1), 1995, pp. 53-54
Authors:
WENGER SL
CUMMINS JH
Citation: Sl. Wenger et Jh. Cummins, FLUORESCENT IN-SITU HYBRIDIZATION FOR EVALUATION OF PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of medical genetics, 57(4), 1995, pp. 639-639
Authors:
SCOTT JA
WENGER SL
STEELE MW
CHAKRAVARTI A
Citation: Ja. Scott et al., DOWN-SYNDROME CONSEQUENT TO A CRYPTIC MATERNAL 12P-21Q-CHROMOSOME TRANSLOCATION, American journal of medical genetics, 56(1), 1995, pp. 67-71
Authors:
KOCOVA M
SIEGEL SF
WENGER SL
LEE PA
NALESNIK M
TRUCCO M
Citation: M. Kocova et al., DETECTION OF Y-CHROMOSOME SEQUENCES IN A 45,X 46,XXQ- PATIENT BY SOUTHERN BLOT ANALYSIS OF PCR-AMPLIFIED DNA AND FLUORESCENT IN-SITU HYBRIDIZATION (FISH)/, American journal of medical genetics, 55(4), 1995, pp. 483-488
Authors:
WENGER SL
STEELE MW
BOONE LY
LENKEY SG
CUMMINS JH
CHEN XQ
Citation: Sl. Wenger et al., BALANCED KARYOTYPES IN 6 ABNORMAL OFFSPRING OF BALANCED RECIPROCAL TRANSLOCATION NORMAL CARRIER PARENTS, American journal of medical genetics, 55(1), 1995, pp. 47-52
Authors:
WENGER SL
Citation: Sl. Wenger, SISTER-CHROMATID EXCHANGE IN PRADER-WILLI-SYNDROME FAMILIES, Clinical genetics, 48(3), 1995, pp. 167-168
Authors:
GIANGRECO CA
STEELE MW
ASTON CE
CUMMINS JH
WENGER SL
Citation: Ca. Giangreco et al., CLINICAL-CRITERIA FOR FRAGILE-X SOUTHERN BLOT DNA DIAGNOSTIC TESTING, American journal of human genetics, 57(4), 1995, pp. 494-494
Authors:
RUBINSTEIN WS
WENGER SL
HOFFMAN RM
MULVIHILL JJ
Citation: Ws. Rubinstein et al., FANCONI-ANEMIA (FA) AND IDIOPATHIC INTERSTITIAL LUNG-DISEASE (ILD), American journal of human genetics, 57(4), 1995, pp. 558-558