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Results: 1-25 | 26-47 |
Results: 26-47/47
EVALUATION OF THE PATIENT WITH IDIOPATHIC MENTAL-RETARDATION
Authors: BODENSTEINER JB SCHAEFER GB
Citation: Jb. Bodensteiner et Gb. Schaefer, EVALUATION OF THE PATIENT WITH IDIOPATHIC MENTAL-RETARDATION, The Journal of neuropsychiatry and clinical neurosciences, 7(3), 1995, pp. 361-370
HYPOPLASIA OF THE CORPUS-CALLOSUM AND CEREBRAL-PALSY
Authors: SHETH RD SCHAEFER GB ORTIZ O KELLER GM BODENSTEINER JB
Citation: Rd. Sheth et al., HYPOPLASIA OF THE CORPUS-CALLOSUM AND CEREBRAL-PALSY, Annals of neurology, 38(3), 1995, pp. 516-516
EXPRESSION OF 72 KDA AND 92 KDA TYPE-IV COLLAGENASES FROM HUMAN GIANT-CELL TUMOR OF BONE
Authors: RAO VH BRIDGE JA NEFF JR SCHAEFER GB BUEHLER BA VISHWANATHA JK POLLOCK RE NICOLSON GL YAMAMOTO M GOKASLAM ZL STETLERSTEVENSON WG SAWAYA R RAO JS
Citation: Vh. Rao et al., EXPRESSION OF 72 KDA AND 92 KDA TYPE-IV COLLAGENASES FROM HUMAN GIANT-CELL TUMOR OF BONE, Clinical & experimental metastasis, 13(6), 1995, pp. 420-426
FAMILIAL INVERTED DUPLICATION 7P
Authors: SCHAEFER GB NOVAK K STEELE D BUEHLER B SMITH S ZALESKI D PICKERING D NELSON M SANGER W
Citation: Gb. Schaefer et al., FAMILIAL INVERTED DUPLICATION 7P, American journal of medical genetics, 56(2), 1995, pp. 184-187
QUANTITATION OF FIBRILLIN IMMUNOFLUORESCENCE IN FIBROBLAST-CULTURES IN THE MARFAN-SYNDROME
Authors: SCHAEFER GB GODFREY M
Citation: Gb. Schaefer et M. Godfrey, QUANTITATION OF FIBRILLIN IMMUNOFLUORESCENCE IN FIBROBLAST-CULTURES IN THE MARFAN-SYNDROME, Clinical genetics, 47(3), 1995, pp. 144-149
HYPOPLASIA OF THE CORPUS-CALLOSUM - A STUDY OF 445 CONSECUTIVE MRI SCANS
Authors: BODENSTEINER J SCHAEFER GB BREEDING L COWAN L
Citation: J. Bodensteiner et al., HYPOPLASIA OF THE CORPUS-CALLOSUM - A STUDY OF 445 CONSECUTIVE MRI SCANS, Journal of child neurology, 9(1), 1994, pp. 47-49
CEREBRAL DYSGENESIS - AN OVERVIEW
Authors: SCHAEFER GB SHETH RD BODENSTEINER JB
Citation: Gb. Schaefer et al., CEREBRAL DYSGENESIS - AN OVERVIEW, Neurologic clinics, 12(4), 1994, pp. 773-788
PEDIATRIC NEUROGENETICS - PREFACE
Authors: SCHAEFER GB BODENSTEINER JB
Citation: Gb. Schaefer et Jb. Bodensteiner, PEDIATRIC NEUROGENETICS - PREFACE, Neurologic clinics, 12(4), 1994, pp. 180000009-180000010
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
HYPOPLASIA OF THE CEREBELLAR VERMIS AND CORPUS-CALLOSUM IN THROMBOCYTOPENIA WITH ABSENT RADIUS SYNDROME ON MRI STUDIES
Authors: MACDONALD MR SCHAEFER GB OLNEY AH PATTON DF
Citation: Mr. Macdonald et al., HYPOPLASIA OF THE CEREBELLAR VERMIS AND CORPUS-CALLOSUM IN THROMBOCYTOPENIA WITH ABSENT RADIUS SYNDROME ON MRI STUDIES, American journal of medical genetics, 50(1), 1994, pp. 46-50
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
LIPIDS AND APOLIPOPROTEINS IN GROWTH HORMONE-DEFICIENT CHILDREN DURING TREATMENT
Authors: SCHAEFER GB GREGER NG FESMIRE JD BLACKETT PR WILSON DP FRINDIK JP
Citation: Gb. Schaefer et al., LIPIDS AND APOLIPOPROTEINS IN GROWTH HORMONE-DEFICIENT CHILDREN DURING TREATMENT, Metabolism, clinical and experimental, 43(12), 1994, pp. 1457-1461
FACIAL MORPHOMETRY OF ECUADORIAN PATIENTS WITH GROWTH-HORMONE RECEPTOR DEFICIENCY LARON SYNDROME
Authors: SCHAEFER GB ROSENBLOOM AL GUEVARAAGUIRRE J CAMPBELL EA ULLRICH F PATIL K FRIAS JL
Citation: Gb. Schaefer et al., FACIAL MORPHOMETRY OF ECUADORIAN PATIENTS WITH GROWTH-HORMONE RECEPTOR DEFICIENCY LARON SYNDROME, Journal of Medical Genetics, 31(8), 1994, pp. 635-639
SUBTLE ANOMALIES OF THE SEPTUM PELLUCIDUM AND NEURODEVELOPMENTAL DEFICITS
Authors: SCHAEFER GB BODENSTEINER JB THOMPSON JN
Citation: Gb. Schaefer et al., SUBTLE ANOMALIES OF THE SEPTUM PELLUCIDUM AND NEURODEVELOPMENTAL DEFICITS, Developmental Medicine and Child Neurology, 36(6), 1994, pp. 554-559
IN-SITU HYBRIDIZATION OF GONADAL TISSUE FROM SEX-CHROMOSOME ANEUPLOIDINDIVIDUALS
Authors: DEBOER J GUTKIN D SEEMAYER T SCHAEFER GB BRIDGE JA
Citation: J. Deboer et al., IN-SITU HYBRIDIZATION OF GONADAL TISSUE FROM SEX-CHROMOSOME ANEUPLOIDINDIVIDUALS, Clinical research, 42(3), 1994, pp. 10000373-10000373
MUTATION ANALYSIS AND HAPLOTYPE CORRELATION FOR 139 CYSTIC-FIBROSIS PATIENTS FROM THE NEBRASKA REGIONAL CYSTIC-FIBROSIS CENTER
Authors: TRAYSTMAN MD SCHULTE N COLOMBO JL SAMMUT PH REILLY P PATEL C ACQUAZZINO D SIMANEK B ANDERSON R KIMBERLING WJ SCHAEFER GB SANGER WG
Citation: Md. Traystman et al., MUTATION ANALYSIS AND HAPLOTYPE CORRELATION FOR 139 CYSTIC-FIBROSIS PATIENTS FROM THE NEBRASKA REGIONAL CYSTIC-FIBROSIS CENTER, Human mutation, 2(1), 1993, pp. 7-15
ELASTIN AND FIBRILLIN MESSENGER-RNA AND PROTEIN-LEVELS IN THE ONTOGENY OF NORMAL HUMAN AORTA
Authors: GODFREY M NEJEZCHLEB PA SCHAEFER GB MINION DJ WANG Y BAXTER BT
Citation: M. Godfrey et al., ELASTIN AND FIBRILLIN MESSENGER-RNA AND PROTEIN-LEVELS IN THE ONTOGENY OF NORMAL HUMAN AORTA, Connective tissue research, 29(1), 1993, pp. 61-69
PATIENT WITH DOUBLE HETEROZYGOSITY FOR ACHONDROPLASIA AND PSEUDOACHONDROPLASIA, WITH COMMENTS ON THESE CONDITIONS AND THE RELATIONSHIP BETWEEN PSEUDOACHONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA, FAIRBANK TYPE
Authors: LANGER LO SCHAEFER GB WADSWORTH DT
Citation: Lo. Langer et al., PATIENT WITH DOUBLE HETEROZYGOSITY FOR ACHONDROPLASIA AND PSEUDOACHONDROPLASIA, WITH COMMENTS ON THESE CONDITIONS AND THE RELATIONSHIP BETWEEN PSEUDOACHONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA, FAIRBANK TYPE, American journal of medical genetics, 47(5), 1993, pp. 772-781
BRAIN MAGNETIC-RESONANCE-IMAGING FINDINGS IN THE OPITZ G BBB SYNDROME- EXTENSION OF THE SPECTRUM OF MIDLINE BRAIN ANOMALIES/
Authors: MACDONALD MR SCHAEFER GB OLNEY AH TAMAYO M FRIAS JL
Citation: Mr. Macdonald et al., BRAIN MAGNETIC-RESONANCE-IMAGING FINDINGS IN THE OPITZ G BBB SYNDROME- EXTENSION OF THE SPECTRUM OF MIDLINE BRAIN ANOMALIES/, American journal of medical genetics, 46(6), 1993, pp. 706-711
MIDLINE CEREBRAL DYSGENESIS, DYSFUNCTION OF THE HYPOTHALAMIC-PITUITARY AXIS, AND FETAL ALCOHOL EFFECTS
Authors: COULTER CL LEECH RW SCHAEFER GB SCHEITHAUER BW BRUMBACK RA
Citation: Cl. Coulter et al., MIDLINE CEREBRAL DYSGENESIS, DYSFUNCTION OF THE HYPOTHALAMIC-PITUITARY AXIS, AND FETAL ALCOHOL EFFECTS, Archives of neurology, 50(7), 1993, pp. 771-775
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
TELEDIAGNOSTIC CONFERENCING
Authors: FEINGOLD M FRIAS J LIN AE SCHAEFER GB HORWITZ M
Citation: M. Feingold et al., TELEDIAGNOSTIC CONFERENCING, American journal of diseases of children [1960], 147(11), 1993, pp. 1196-1196
Risultati: 1-25 | 26-47 |