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Results: 1-17 |
Results: 17
CLASSIFYING SEX-BIASED CONGENITAL-ANOMALIES
Authors: LUBINSKY MS
Citation: Ms. Lubinsky, CLASSIFYING SEX-BIASED CONGENITAL-ANOMALIES, American journal of medical genetics, 69(3), 1997, pp. 225-228
DECREASED MATERNAL AGE WITH HYDRANENCEPHALY
Authors: LUBINSKY MS ADKINS W KAVEGGIA EG
Citation: Ms. Lubinsky et al., DECREASED MATERNAL AGE WITH HYDRANENCEPHALY, American journal of medical genetics, 69(3), 1997, pp. 232-234
HYPOTHESIS - SEPTO-OPTIC DYSPLASIA IS A VASCULAR DISRUPTION SEQUENCE
Authors: LUBINSKY MS
Citation: Ms. Lubinsky, HYPOTHESIS - SEPTO-OPTIC DYSPLASIA IS A VASCULAR DISRUPTION SEQUENCE, American journal of medical genetics, 69(3), 1997, pp. 235-236
ASSOCIATION OF PRENATAL VASCULAR DISRUPTIONS WITH DECREASED MATERNAL AGE
Authors: LUBINSKY MS
Citation: Ms. Lubinsky, ASSOCIATION OF PRENATAL VASCULAR DISRUPTIONS WITH DECREASED MATERNAL AGE, American journal of medical genetics, 69(3), 1997, pp. 237-239
DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE-1A NEUROPATHY
Authors: ROA BB GREENBERG F GUNARATNE P SAUER CM LUBINSKY MS KOZMA C MECK JM MAGENIS RE SHAFFER LG LUPSKI JR
Citation: Bb. Roa et al., DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE-1A NEUROPATHY, Human genetics, 97(5), 1996, pp. 642-649
DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE 1A NEUROPATHY
Authors: ROA BB GREENBERG F GUNARATNE P SAUER CM LUBINSKY MS KOZMA C MECK JM MAGENIS RE SHAFFER LG LUPSKI JR
Citation: Bb. Roa et al., DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE 1A NEUROPATHY, American journal of human genetics, 57(4), 1995, pp. 171-171
LOWER AGE-SPECIFIC RATES FOR GASTROSCHISIS IN CALIFORNIA BLACKS THAN IN WHITES - AN UNEXPECTED RELATIONSHIP OF RACE AND DECREASED MATERNAL AGE EFFECTS IN A POPULATION-BASED STUDY
Authors: LUBINSKY MS TORFS C BATESON T
Citation: Ms. Lubinsky et al., LOWER AGE-SPECIFIC RATES FOR GASTROSCHISIS IN CALIFORNIA BLACKS THAN IN WHITES - AN UNEXPECTED RELATIONSHIP OF RACE AND DECREASED MATERNAL AGE EFFECTS IN A POPULATION-BASED STUDY, American journal of human genetics, 57(4), 1995, pp. 1845-1845
LINKAGE OF A GENE CAUSING FAMILIAL HOLOPROSENCEPHALY (HPE) TO CHROMOSOME 7Q36
Authors: MUENKE M GURRIERI F YI D BAY C COLLINS AL JOHNSON VP HENNEKAM RCM SCHAEFER GB LUBINSKY MS MOORE CA DOBYNS WB MURRAY JC PRICE RA
Citation: M. Muenke et al., LINKAGE OF A GENE CAUSING FAMILIAL HOLOPROSENCEPHALY (HPE) TO CHROMOSOME 7Q36, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 70-71
URTICARIA PIGMENTOSA AND NAGER SYNDROME
Authors: NAKATA ML LUBINSKY MS ESTERLY NB
Citation: Ml. Nakata et al., URTICARIA PIGMENTOSA AND NAGER SYNDROME, Journal of the American Academy of Dermatology, 30(5), 1994, pp. 795-797
VON VOSS-CHERSTVOY SYNDROME - A VARIABLE PERINATALLY LETHAL SYNDROME OF MULTIPLE CONGENITAL-ANOMALIES
Authors: LUBINSKY MS KAHLER SG SPEER IE HOYME HE KIRILLOVA IA LURIE IW
Citation: Ms. Lubinsky et al., VON VOSS-CHERSTVOY SYNDROME - A VARIABLE PERINATALLY LETHAL SYNDROME OF MULTIPLE CONGENITAL-ANOMALIES, American journal of medical genetics, 52(3), 1994, pp. 272-278
PROPERTIES OF ASSOCIATIONS - IDENTITY, NATURE, AND CLINICAL-CRITERIA,WITH A COMMENTARY ON WHY CHARGE AND GOLDENHAR ARE NOT ASSOCIATIONS
Authors: LUBINSKY MS
Citation: Ms. Lubinsky, PROPERTIES OF ASSOCIATIONS - IDENTITY, NATURE, AND CLINICAL-CRITERIA,WITH A COMMENTARY ON WHY CHARGE AND GOLDENHAR ARE NOT ASSOCIATIONS, American journal of medical genetics, 49(1), 1994, pp. 21-25
LINKAGE OF A HUMAN BRAIN MALFORMATION, FAMILIAL HOLOPROSENCEPHALY, TOCHROMOSOME-7 AND EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: MUENKE M GURRIERI F BAY C YI DH COLLINS AL JOHNSON VP HENNEKAM RCM SCHAEFER GB WEIK LA LUBINSKY MS DAACKHIRSCH S MOORE CA DOBYNS WB MURRAY JC PRICE RA
Citation: M. Muenke et al., LINKAGE OF A HUMAN BRAIN MALFORMATION, FAMILIAL HOLOPROSENCEPHALY, TOCHROMOSOME-7 AND EVIDENCE FOR GENETIC-HETEROGENEITY, Proceedings of the National Academy of Sciences of the United Statesof America, 91(17), 1994, pp. 8102-8106
NEONATAL HYPOTONIA AND CARDIOMYOPATHY SECONDARY TO TYPE-IV GLYCOGENOSIS
Authors: TANG TT SEGURA AD CHEN YT RICCI LM FRANCIOSI RA SPLAINGARD ML LUBINSKY MS
Citation: Tt. Tang et al., NEONATAL HYPOTONIA AND CARDIOMYOPATHY SECONDARY TO TYPE-IV GLYCOGENOSIS, Acta Neuropathologica, 87(5), 1994, pp. 531-536
DEGENERATE HEREDITY - THE HISTORY OF A DOCTRINE IN MEDICINE AND BIOLOGY
Authors: LUBINSKY MS
Citation: Ms. Lubinsky, DEGENERATE HEREDITY - THE HISTORY OF A DOCTRINE IN MEDICINE AND BIOLOGY, Perspectives in biology and medicine, 37(1), 1993, pp. 74-90
LINKAGE OF FAMILIAL HOLOPROSENCEPHALY TO CHROMOSOME-7Q36 - CLINICAL AND MOLECULAR STUDIES
Authors: MUENKE M GURRIERI F YI D BAY C COLLINS AL JOHNSON VP HENNEKAM RCM SCHAEFER GB WEIK J LUBINSKY MS DAACKHERSH S MOORE CA DOBYNS WB MURRAY JC PRICE RA
Citation: M. Muenke et al., LINKAGE OF FAMILIAL HOLOPROSENCEPHALY TO CHROMOSOME-7Q36 - CLINICAL AND MOLECULAR STUDIES, American journal of human genetics, 53(3), 1993, pp. 1048-1048
MINIMUM GUIDELINES FOR THE DELIVERY OF CLINICAL GENETICS SERVICES
Authors: WEAVER DD BAKER D THEOBALD M COHEN F KING RA KRUEGER S LAXOVA R LUBINSKY MS
Citation: Dd. Weaver et al., MINIMUM GUIDELINES FOR THE DELIVERY OF CLINICAL GENETICS SERVICES, American journal of human genetics, 53(1), 1993, pp. 287-289
GM(1)-GANGLIOSIDOSIS TYPE-1 INVOLVING THE CUTANEOUS VASCULAR ENDOTHELIAL-CELLS IN A BLACK INFANT WITH MULTIPLE ECTOPIC MONGOLIAN SPOTS
Authors: TANG TT ESTERLY NB LUBINSKY MS OECHLER HW HARB JM FRANCIOSI RA
Citation: Tt. Tang et al., GM(1)-GANGLIOSIDOSIS TYPE-1 INVOLVING THE CUTANEOUS VASCULAR ENDOTHELIAL-CELLS IN A BLACK INFANT WITH MULTIPLE ECTOPIC MONGOLIAN SPOTS, Acta dermato-venereologica, 73(6), 1993, pp. 412-415
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