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Results: 1-25 | 26-50 | 51-61
Results: 1-25/61
HLA-DQB1 AND HLA-DPB1 GENOTYPES IN FAMILIAL SARCOIDOSIS
Authors: SCHURMANN M BEIN G KIRSTEN D SCHLAAK M MULLERQUERNHEIM J SCHWINGER E
Citation: M. Schurmann et al., HLA-DQB1 AND HLA-DPB1 GENOTYPES IN FAMILIAL SARCOIDOSIS, Respiratory medicine, 92(4), 1998, pp. 649-652
EYE TRACKING DYSFUNCTION (ETD) AS A MEASURABLE INDICATOR FOR THE VULNERABILITY TO SCHIZOPHRENIA
Authors: LENCER R NOLTE A KRECKER K SCHWINGER E AROLT V
Citation: R. Lencer et al., EYE TRACKING DYSFUNCTION (ETD) AS A MEASURABLE INDICATOR FOR THE VULNERABILITY TO SCHIZOPHRENIA, Schizophrenia research, 29(1-2), 1998, pp. 116-116
LINKAGE OF EYE TRACKING DYSFUNCTION TO DNA-MARKERS ON CHROMOSOME 6P21IN SCHIZOPHRENIA
Authors: AROLT V LENCER R SCHURMANN M PURMANN S KRECKER K SCHWINGER E
Citation: V. Arolt et al., LINKAGE OF EYE TRACKING DYSFUNCTION TO DNA-MARKERS ON CHROMOSOME 6P21IN SCHIZOPHRENIA, Schizophrenia research, 29(1-2), 1998, pp. 138-139
MUTATION OF THE START CODON IN THE FRDA1 GENE - LINKAGE ANALYSIS OF 3PEDIGREES WITH THE ATG TO ATT TRANSVERSION PAINTS TO A UNIQUE COMMON ANCESTOR
Authors: ZUHLKE C LACCONE F COSSEE M KOHLSCHUTTER A KOENIG M SCHWINGER E
Citation: C. Zuhlke et al., MUTATION OF THE START CODON IN THE FRDA1 GENE - LINKAGE ANALYSIS OF 3PEDIGREES WITH THE ATG TO ATT TRANSVERSION PAINTS TO A UNIQUE COMMON ANCESTOR, Human genetics, 103(1), 1998, pp. 102-105
STATEMENT REGARDING ABORTION SUBSEQUENT TO PRENATAL DIAGNOSTIC STUDY
Authors: BACHMANN KD BERG D DUDENHAUSEN JW GRAUEL EL GRIMM T GRUNDEL J HEPP H HOLZGREVE W POHLANDT F SCHWINGER E VONSTOCKHAUSEN HB WOLFF G WOLFSLAST G WOLLERSHEIM RAU WOOPEN C WUERMELING HB
Citation: Kd. Bachmann et al., STATEMENT REGARDING ABORTION SUBSEQUENT TO PRENATAL DIAGNOSTIC STUDY, Monatsschrift fur Kinderheilkunde, 146(4), 1998, pp. 347-350
PREIMPLANTATION DIAGNOSIS IN HUMAN-GENETI CS
Authors: SCHWINGER E
Citation: E. Schwinger, PREIMPLANTATION DIAGNOSIS IN HUMAN-GENETI CS, Der Gynakologe, 31(4), 1998, pp. 360-363
NEURAL-TUBE DEFECTS IN CHROMOSOMALLY NORMAL AND ABNORMAL HUMAN EMBRYOS
Authors: COERDT W MILLER K HOLZGREVE W RAUSKOLB R SCHWINGER E REHDER H
Citation: W. Coerdt et al., NEURAL-TUBE DEFECTS IN CHROMOSOMALLY NORMAL AND ABNORMAL HUMAN EMBRYOS, Ultrasound in obstetrics & gynecology, 10(6), 1997, pp. 410-415
CAG REPEAT ANALYSES IN FROZEN AND FORMALIN-FIXED TISSUES FOLLOWING PRIMER EXTENSION PREAMPLIFICATION FOR EVALUATION OF MITOTIC INSTABILITY OF EXPANDED SCA1 ALLELES
Authors: ZUHLKE C HELLENBROICH Y SCHAAFF F GEHLKEN U WESSEL K SCHUBERT T CERVOSNAVARRO J PICKARTZ H SCHWINGER E
Citation: C. Zuhlke et al., CAG REPEAT ANALYSES IN FROZEN AND FORMALIN-FIXED TISSUES FOLLOWING PRIMER EXTENSION PREAMPLIFICATION FOR EVALUATION OF MITOTIC INSTABILITY OF EXPANDED SCA1 ALLELES, Human genetics, 100(3-4), 1997, pp. 339-344
ASSISTED FERTILIZATION IN CASES OF CHROMOSOMAL ABNORMALITY
Authors: KUPKER W SCHWINGER E ZIKULNIG L ALHASANI S LUDWIG M DIEDRICH C DIEDRICH K
Citation: W. Kupker et al., ASSISTED FERTILIZATION IN CASES OF CHROMOSOMAL ABNORMALITY, Human reproduction, 12, 1997, pp. 164-164
LINKAGE ANALYSES OF EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q
Authors: LENCER R AROTT V PURMANN S SCHURMANN M MULLERMYHSOK B NOLTE A KRECKER K SCHWINGER E
Citation: R. Lencer et al., LINKAGE ANALYSES OF EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q, American journal of medical genetics, 74(6), 1997, pp. 595-595
LINKAGE ANALYSES OF EYE-TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q
Authors: LENCER R AROLT V PURMANN S SCHURMANN M MULLERMYHSOK B NOLTE A KRECKER K SCHWINGER E
Citation: R. Lencer et al., LINKAGE ANALYSES OF EYE-TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q, American journal of medical genetics, 74(6), 1997, pp. 666-666
MOLECULAR CYTOGENETIC DIAGNOSTICS IN SPERM
Authors: MENNICKE K DIERCKS P SCHLIEKER H BALSPRATSCH M ALHASANI S DIEDRICH K SCHWINGER E
Citation: K. Mennicke et al., MOLECULAR CYTOGENETIC DIAGNOSTICS IN SPERM, International journal of andrology, 20, 1997, pp. 11-19
GENETIC-ASPECTS OF CONGENITAL FETAL CARDI AC DISEASE
Authors: MENNICKE K SCHWINGER E
Citation: K. Mennicke et E. Schwinger, GENETIC-ASPECTS OF CONGENITAL FETAL CARDI AC DISEASE, Der Gynakologe, 30(3), 1997, pp. 181-189
ASSISTED FERTILIZATION IN CASES OF CHROMOSOMAL-ABNORMALITIES
Authors: KUPKER W SCHWINGER E ZIKULNIG L MENNICKE K ALHASANI S LUDWIG M FELBERBAUM R DIEDRICH C DIEDRICH K
Citation: W. Kupker et al., ASSISTED FERTILIZATION IN CASES OF CHROMOSOMAL-ABNORMALITIES, Fertility and sterility, 1997, pp. 162-162
PRIMED IN-SITU LABELING (PRINS) FOR THE DETECTION OF SINGLE-COPY SEQUENCES AND GENE POLYMORPHISM ON HUMAN-CHROMOSOMES
Authors: MENNICKE KC HARRER T SCHUERMANN M MUELLER A SCHWINGER E
Citation: Kc. Mennicke et al., PRIMED IN-SITU LABELING (PRINS) FOR THE DETECTION OF SINGLE-COPY SEQUENCES AND GENE POLYMORPHISM ON HUMAN-CHROMOSOMES, American journal of human genetics, 61(4), 1997, pp. 762-762
EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA
Authors: AROLT V LENCER R NOLTE A PINNOW M SCHWINGER E
Citation: V. Arolt et al., EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA, European archives of psychiatry and clinical neuroscience, 246(4), 1996, pp. 175-181
ANALYSIS OF SEX AND DELTA-F508 IN SINGLE AMNIOCYTES USING PRIMER EXTENSION PREAMPLIFICATION
Authors: SCHAAFF F WEDEMANN H SCHWINGER E
Citation: F. Schaaff et al., ANALYSIS OF SEX AND DELTA-F508 IN SINGLE AMNIOCYTES USING PRIMER EXTENSION PREAMPLIFICATION, Human genetics, 98(2), 1996, pp. 158-161
ASSISTED REPRODUCTIVE TECHNIQUES - ARE WE AVOIDING THE GENETIC ISSUES
Authors: BASCHAT AA SCHWINGER E DIEDRICH K
Citation: Aa. Baschat et al., ASSISTED REPRODUCTIVE TECHNIQUES - ARE WE AVOIDING THE GENETIC ISSUES, Human reproduction, 11(5), 1996, pp. 926-928
RESULTS OF CYTOGENETIC ANALYSIS IN MEN WITH SEVERE SUBFERTILITY PRIORTO INTRACYTOPLASMIC SPERM INJECTION
Authors: BASCHAT AA KUPKER W ALHASANI S DIEDRICH K SCHWINGER E
Citation: Aa. Baschat et al., RESULTS OF CYTOGENETIC ANALYSIS IN MEN WITH SEVERE SUBFERTILITY PRIORTO INTRACYTOPLASMIC SPERM INJECTION, Human reproduction, 11(2), 1996, pp. 330-333
EYE TRACKING DYSFUNCTION IS A PUTATIVE PHENOTYPIC SUSCEPTIBILITY MARKER OF SCHIZOPHRENIA AND MAPS TO A LOCUS ON CHROMOSOME 6P IN FAMILIES WITH MULTIPLE OCCURRENCE OF THE DISEASE
Authors: AROLT V LENCER R NOLTE A MULLERMYHSOK B PURMANN S SCHURMANN M LEUTELT J PINNOW M SCHWINGER E
Citation: V. Arolt et al., EYE TRACKING DYSFUNCTION IS A PUTATIVE PHENOTYPIC SUSCEPTIBILITY MARKER OF SCHIZOPHRENIA AND MAPS TO A LOCUS ON CHROMOSOME 6P IN FAMILIES WITH MULTIPLE OCCURRENCE OF THE DISEASE, American journal of medical genetics, 67(6), 1996, pp. 564-579
SHORT STATURE IN A MOTHER AND DAUGHTER WITH TERMINAL DELETION OF XP22.3
Authors: SCHWINGER E KIRSCHSTEIN M GREIWE M KONERMANN T ORTH U GAL A
Citation: E. Schwinger et al., SHORT STATURE IN A MOTHER AND DAUGHTER WITH TERMINAL DELETION OF XP22.3, American journal of medical genetics, 63(1), 1996, pp. 239-242
VACTERL WITH HYDROCEPHALUS AND BRANCHIAL ARCH DEFECTS - PRENATAL, CLINICAL, AND AUTOPSY FINDINGS IN 2 BROTHERS
Authors: FROSTER UG WALLNER SJ REUSCHE E SCHWINGER E REHDER H
Citation: Ug. Froster et al., VACTERL WITH HYDROCEPHALUS AND BRANCHIAL ARCH DEFECTS - PRENATAL, CLINICAL, AND AUTOPSY FINDINGS IN 2 BROTHERS, American journal of medical genetics, 62(2), 1996, pp. 169-172
5 NOVEL MUTATIONS IN THE L1CAM GENE IN FAMILIES WITH X-LINKED HYDROCEPHALUS
Authors: GU SM ORTH U VESKE A ENDERS H KLUNDER K SCHLOSSER M ENGEL W SCHWINGER E GAL A
Citation: Sm. Gu et al., 5 NOVEL MUTATIONS IN THE L1CAM GENE IN FAMILIES WITH X-LINKED HYDROCEPHALUS, Journal of Medical Genetics, 33(2), 1996, pp. 103-106
FAMILIAL OCCURRENCE OF OCULOAURICULOVERTE BRAL DYSPLASIA AND FRANCESCHETTI SYNDROME
Authors: BESTELMEYER U WEERDA H SIEGERT R GREIWE M SCHWINGER E
Citation: U. Bestelmeyer et al., FAMILIAL OCCURRENCE OF OCULOAURICULOVERTE BRAL DYSPLASIA AND FRANCESCHETTI SYNDROME, HNO. Hals-, Nasen-, Ohrenarzte, 44(8), 1996, pp. 452-455
JUMPING TRANSLOCATION IN A PHENOTYPICALLY NORMAL FEMALE
Authors: VONBALLESTREM CL BOAVIDA MG ZUTHER C CARREIRO MH DAVID D GAL A SCHWINGER E
Citation: Cl. Vonballestrem et al., JUMPING TRANSLOCATION IN A PHENOTYPICALLY NORMAL FEMALE, Clinical genetics, 49(3), 1996, pp. 156-159
Risultati: 1-25 | 26-50 | 51-61