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Results: 1-25 | 26-50 | 51-61
Results: 26-50/61
PROGRESS IN THE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES
Authors: MOISES HW YANG L KRISTBJARNARSON H BYERLEY W MACCIARDI F AROLT V BLACKWOOD D ASCHAUER HN HWU HG WEISSENBACH J SCHWINGER E GOTTESMAN II WETTERBERG L HELGASON T
Citation: Hw. Moises et al., PROGRESS IN THE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES, Biological psychiatry, 39(7), 1996, pp. 394-394
CHROMOSOMAL MOSAICISM 45,X 46,XY/47,XYY A S A CAUSE OF HYPERGONADOTROPIC HYPOGONADISM FIRST DIAGNOSED IN LATE MIDDLE-AGE/
Authors: KREFT B GREIWE M SCHWINGER E PETERS A
Citation: B. Kreft et al., CHROMOSOMAL MOSAICISM 45,X 46,XY/47,XYY A S A CAUSE OF HYPERGONADOTROPIC HYPOGONADISM FIRST DIAGNOSED IN LATE MIDDLE-AGE/, Deutsche Medizinische Wochenschrift, 120(33), 1995, pp. 1114-1117
AN INTERNATIONAL 2-STAGE GENOME-WIDE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES
Authors: MOISES HW YANG L KRISTBJARNARSON H WIESE C BYERLEY W MACCIARDI F AROLT V BLACKWOOD D LIU X SJOGREN S ASCHAUER HN HWU HG JANG K LIVESLEY WJ KENNEDY JL ZOEGA T IVARSSON O BUI MT YU MH HAVSTEEN B COMMENGES D WEISSENBACH J SCHWINGER E GOTTESMAN II PAKSTIS AJ WETTERBERG L KIDD KK HELGASON T
Citation: Hw. Moises et al., AN INTERNATIONAL 2-STAGE GENOME-WIDE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES, Nature genetics, 11(3), 1995, pp. 321-324
MUCOPOLYSACCHARIDOSIS TYPE-I - IDENTIFICATION OF 13 NOVEL MUTATIONS OF THE ALPHA-L-IDURONIDASE GENE
Authors: BUNGE S KLEIJER WJ STEGLICH C BECK M SCHWINGER E GAL A
Citation: S. Bunge et al., MUCOPOLYSACCHARIDOSIS TYPE-I - IDENTIFICATION OF 13 NOVEL MUTATIONS OF THE ALPHA-L-IDURONIDASE GENE, Human mutation, 6(1), 1995, pp. 91-94
MUTATIONS OF THE IDURONATE-2-SULFATASE GENE IN 12 POLISH PATIENTS WITH MUCOPOLYSACCHARIDOSIS TYPE-11 (HUNTER-SYNDROME)
Authors: POPOWSKA E RATHMANN M TYLKISZYMANSKA A BUNGE S STEGLICH C SCHWINGER E GAL A
Citation: E. Popowska et al., MUTATIONS OF THE IDURONATE-2-SULFATASE GENE IN 12 POLISH PATIENTS WITH MUCOPOLYSACCHARIDOSIS TYPE-11 (HUNTER-SYNDROME), Human mutation, 5(1), 1995, pp. 97-100
COMMON CFTR MUTATIONS ARE NOT LIKELY TO PREDISPOSE TO CHRONIC-BRONCHITIS IN NORTHERN GERMANY
Authors: ARTLICH A BOYSEN A BUNGE S ENTZIAN P SCHLAAK M SCHWINGER E
Citation: A. Artlich et al., COMMON CFTR MUTATIONS ARE NOT LIKELY TO PREDISPOSE TO CHRONIC-BRONCHITIS IN NORTHERN GERMANY, Human genetics, 95(2), 1995, pp. 226-228
EVIDENCE FOR AN IDURONATE-SULFATASE PSEUDOGENE NEAR THE FUNCTIONAL HUNTER SYNDROME GENE IN XQ27.3-Q28
Authors: RATHMANN M BUNGE S STEGLICH C SCHWINGER E GAL A
Citation: M. Rathmann et al., EVIDENCE FOR AN IDURONATE-SULFATASE PSEUDOGENE NEAR THE FUNCTIONAL HUNTER SYNDROME GENE IN XQ27.3-Q28, Human genetics, 95(1), 1995, pp. 34-38
FREQUENCY OF COMMON CYSTIC-FIBROSIS GENE-MUTATIONS IN CHRONIC-BRONCHITIS PATIENTS
Authors: ENTZIAN P MULLER E BOYSEN A ARTLICH A SCHWINGER E SCHLAAK M
Citation: P. Entzian et al., FREQUENCY OF COMMON CYSTIC-FIBROSIS GENE-MUTATIONS IN CHRONIC-BRONCHITIS PATIENTS, Scandinavian journal of clinical & laboratory investigation, 55(3), 1995, pp. 263-266
CULTURAL DEMAND FOR CONSIDERATENESS - FAM ILIAL LIFE COMPANIONSHIP AND THE RESPONSIBILITY OF POLITICAL REGULATIONS
Authors: SCHWINGER E
Citation: E. Schwinger, CULTURAL DEMAND FOR CONSIDERATENESS - FAM ILIAL LIFE COMPANIONSHIP AND THE RESPONSIBILITY OF POLITICAL REGULATIONS, Deutsche Zeitschrift fur Philosophie, 43(6), 1995, pp. 1005-1018
RACE HYGIENE IN NAZI GERMANY
Authors: PANDER HJ SCHWINGER E
Citation: Hj. Pander et E. Schwinger, RACE HYGIENE IN NAZI GERMANY, American journal of human genetics, 56(5), 1995, pp. 1245-1246
HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS (VOL 7,PG 64, 1994)
Authors: GAL A ORTH U BAEHR W SCHWINGER E ROSENBERG T
Citation: A. Gal et al., HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS (VOL 7,PG 64, 1994), Nature genetics, 7(4), 1994, pp. 551-551
HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS
Authors: GAL A ORTH U BAEHR W SCHWINGER E ROSENBERG T
Citation: A. Gal et al., HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS, Nature genetics, 7(1), 1994, pp. 64-68
X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY - VALINE-38-METHIONINE SUBSTITUTION OF CONNEXIN-32
Authors: ORTH U FAIRWEATHER N EXLER MC SCHWINGER E GAL A
Citation: U. Orth et al., X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY - VALINE-38-METHIONINE SUBSTITUTION OF CONNEXIN-32, Human molecular genetics, 3(9), 1994, pp. 1699-1700
MUCOPOLYSACCHARIDOSIS TYPE-I - IDENTIFICATION OF 8 NOVEL MUTATIONS AND DETERMINATION OF THE FREQUENCY OF THE 2 COMMON ALPHA-1-IDURONIDASE MUTATIONS (W402X AND Q70X) AMONG EUROPEAN PATIENTS
Authors: BUNGE S KLEIJER WJ STEGLICH C BECK M ZUTHER C MORRIS CP SCHWINGER E HOPWOOD JJ SCOTT HS GAL A
Citation: S. Bunge et al., MUCOPOLYSACCHARIDOSIS TYPE-I - IDENTIFICATION OF 8 NOVEL MUTATIONS AND DETERMINATION OF THE FREQUENCY OF THE 2 COMMON ALPHA-1-IDURONIDASE MUTATIONS (W402X AND Q70X) AMONG EUROPEAN PATIENTS, Human molecular genetics, 3(6), 1994, pp. 861-866
GENE FOR AUTOSOMAL-DOMINANT CONGENITAL STATIONARY NIGHT BLINDNESS MAPS TO THE SAME REGION AS THE GENE FOR THE BETA-SUBUNIT OF THE ROD PHOTORECEPTOR CGMP PHOSPHODIESTERASE (PDEB) IN CHROMOSOME 4P16.3
Authors: GAL A XU SY PICZENIK Y EIBERG H DUVIGNEAU C SCHWINGER E ROSENBERG T
Citation: A. Gal et al., GENE FOR AUTOSOMAL-DOMINANT CONGENITAL STATIONARY NIGHT BLINDNESS MAPS TO THE SAME REGION AS THE GENE FOR THE BETA-SUBUNIT OF THE ROD PHOTORECEPTOR CGMP PHOSPHODIESTERASE (PDEB) IN CHROMOSOME 4P16.3, Human molecular genetics, 3(2), 1994, pp. 323-325
MISSENSE MUTATIONS ARE FREQUENT IN THE GENE FOR X-CHROMOSOMAL ADRENOLEUKODYSTROPHY (ALD)
Authors: FUCHS S SARDE CO WEDEMANN H SCHWINGER E MANDEL JL GAL A
Citation: S. Fuchs et al., MISSENSE MUTATIONS ARE FREQUENT IN THE GENE FOR X-CHROMOSOMAL ADRENOLEUKODYSTROPHY (ALD), Human molecular genetics, 3(10), 1994, pp. 1903-1905
MAPPING OF THE AUTOSOMAL-DOMINANT EXUDATIVE VITREORETINOPATHY LOCUS (EVR1) BY MULTIPOINT LINKAGE ANALYSIS IN 4 FAMILIES
Authors: MULLER B ORTH U VANNOUHUYS CE DUVIGNEAU C FUHRMANN C SCHWINGER E LAQUA H GAL A
Citation: B. Muller et al., MAPPING OF THE AUTOSOMAL-DOMINANT EXUDATIVE VITREORETINOPATHY LOCUS (EVR1) BY MULTIPOINT LINKAGE ANALYSIS IN 4 FAMILIES, Genomics, 20(2), 1994, pp. 317-319
D3S1229 AND D3S1246 CORRESPOND TO THE SAME DINUCLEOTIDE REPEAT POLYMORPHISM
Authors: SCHURMANN M LEUTELT J SCHWINGER E GAL A
Citation: M. Schurmann et al., D3S1229 AND D3S1246 CORRESPOND TO THE SAME DINUCLEOTIDE REPEAT POLYMORPHISM, Human genetics, 93(2), 1994, pp. 226-227
TERATOGENIC EFFECTS IN A CASE OF MATERNAL TREATMENT FOR ACUTE MYELOCYTIC - LEUKEMIA NEONATAL AND INFANTILE COURSE
Authors: ARTLICH A MOLLER J TSCHAKALOFF A SCHWINGER E KRUSE K GORTNER L
Citation: A. Artlich et al., TERATOGENIC EFFECTS IN A CASE OF MATERNAL TREATMENT FOR ACUTE MYELOCYTIC - LEUKEMIA NEONATAL AND INFANTILE COURSE, European journal of pediatrics, 153(7), 1994, pp. 488-491
MOLECULAR CHARACTERIZATION OF THE ANDROGEN RECEPTOR GENE IN BOYS WITHHYPOSPADIAS
Authors: HIORT O KLAUBER G CENDRON M SINNECKER GHG KEIM L SCHWINGER E WOLFE HJ YANDELL DW
Citation: O. Hiort et al., MOLECULAR CHARACTERIZATION OF THE ANDROGEN RECEPTOR GENE IN BOYS WITHHYPOSPADIAS, European journal of pediatrics, 153(5), 1994, pp. 317-321
INTRAVENOUS IMMUNOGLOBULIN IN THE PREVENTION OF RECURRENT MISCARRIAGE
Authors: ZINGSEM J ECKSTEIN R MALLMANN P CHRONIDES A DIEKAMP U DOMKE N NAUMANN C SAREMBE B BLASCZYK R GROSSEWILDE H SALEM C FISCHER WM KOHLER S HOLZBERGER G WIEGRATZ I TAUBERT HD MUELLERECKHARDT G POLTEN B LATTERMANN A MELK A BOTZ A THEISS H HEINE O KUNZEL W GERHARD I KOHL C OPELZ G METTLER L WESTPHAL E NEPPERT J GUNTHER W BOLTE A PFEIFFER R ALEXANDER H FROSTERISKENIUS U OBERHEUSER F BEIN G KIRCHNER H WESTERMANN R DEICHERT U REHDER H MEHRAEIN Y SCHWINGER E WALLER H WALLER M KARL M MOHRPENNERT A WEBER E EMONS G METZNER G
Citation: J. Zingsem et al., INTRAVENOUS IMMUNOGLOBULIN IN THE PREVENTION OF RECURRENT MISCARRIAGE, British journal of obstetrics and gynaecology, 101(12), 1994, pp. 1072-1077
LINKAGE ANALYSIS IN FAMILIES WITH LOWE SYNDROME MAPS OCRL DISTAL TO DXS42
Authors: ORTH U ROSENKRANZ W SCHWINGER E GAL A
Citation: U. Orth et al., LINKAGE ANALYSIS IN FAMILIES WITH LOWE SYNDROME MAPS OCRL DISTAL TO DXS42, Cytogenetics and cell genetics, 67(4), 1994, pp. 346-346
TERATOGENIC EFFECTS IN A CASE OF MATERNAL TREATMENT FOR ACUTE LYMPHOBLASTIC-LEUKEMIA (ALL)
Authors: ARTLICH A MOLLER J TSCHAKALOFF A SCHWINGER E KRUSE K GORTNER L
Citation: A. Artlich et al., TERATOGENIC EFFECTS IN A CASE OF MATERNAL TREATMENT FOR ACUTE LYMPHOBLASTIC-LEUKEMIA (ALL), Pediatric research, 35(2), 1994, pp. 260-260
MULVIHILL-SMITH SYNDROME - CASE-REPORT AND REVIEW
Authors: BARTSCH O TYMPNER KD SCHWINGER E GORLIN RJ
Citation: O. Bartsch et al., MULVIHILL-SMITH SYNDROME - CASE-REPORT AND REVIEW, Journal of Medical Genetics, 31(9), 1994, pp. 707-711
COMPENSATORY UNIPARENTAL DISOMY OF CHROMOSOME-21 IN 2 CASES
Authors: BARTSCH O PETERSEN MB STUHLMANN I MAU G FRANTZEN M SCHWINGER E ANTONARAKIS SE MIKKELSEN M
Citation: O. Bartsch et al., COMPENSATORY UNIPARENTAL DISOMY OF CHROMOSOME-21 IN 2 CASES, Journal of Medical Genetics, 31(7), 1994, pp. 534-540
Risultati: 1-25 | 26-50 | 51-61