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Results: 1-14 |
Results: 14
PRENATAL-DIAGNOSIS IN IVF PREGNANCIES - AN INDICATION FOR PREIMPLANTATION GENETICS
Authors: BILENOGLU O BASARAN S YUKSEL A BASAK AN
Citation: O. Bilenoglu et al., PRENATAL-DIAGNOSIS IN IVF PREGNANCIES - AN INDICATION FOR PREIMPLANTATION GENETICS, European journal of human genetics, 6, 1998, pp. 4110-4110
AN UNUSUAL TRANSLOCATION BETWEEN 12TEL AND 14Q11 IN A LARGE KINDRED
Authors: PALANDUZ S USTEK D KARAMAN B OZTURK S CEFLE K BASARAN S
Citation: S. Palanduz et al., AN UNUSUAL TRANSLOCATION BETWEEN 12TEL AND 14Q11 IN A LARGE KINDRED, Hereditas, 128(3), 1998, pp. 231-234
THE IDENTIFICATION OF DE-NOVO STRUCTURAL CHROMOSOME-ABNORMALITIES BY FISH
Authors: KARAMAN B BASARAN S KILIC G AYTAN M KAYSERILI H APAK MY
Citation: B. Karaman et al., THE IDENTIFICATION OF DE-NOVO STRUCTURAL CHROMOSOME-ABNORMALITIES BY FISH, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 23-23
CYTOGENETIC EVALUATION OF FETAL BLOOD-SAMPLES IN FETUSES WITH PATHOLOGICAL ULTRASOUND FINDINGS
Authors: KILIC G BASARAN S YUKSEL A IBRAHIMOGLU L APAK MY
Citation: G. Kilic et al., CYTOGENETIC EVALUATION OF FETAL BLOOD-SAMPLES IN FETUSES WITH PATHOLOGICAL ULTRASOUND FINDINGS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 156-156
IDENTIFICATION OF THE PARENTAL ORIGIN OF POLYSOMY IN 2 49,XXXXY CASES
Authors: CELIK A ERASLAN S GOKGOZ N ILGIN H BASARAN S BOKESOY I KAYSERILI H APAK MY KIRDAR B
Citation: A. Celik et al., IDENTIFICATION OF THE PARENTAL ORIGIN OF POLYSOMY IN 2 49,XXXXY CASES, Clinical genetics, 51(6), 1997, pp. 426-429
ISOCHROMOSOME 18P RESULTS FROM MATERNAL MEIOSIS-II NONDISJUNCTION
Authors: KOTZOT D BUNDSCHERER G BERNASCONI F BRECEVIC L LURIE IW BASARAN S BACCICCHETTI C HOLLER A CASTELLAN C BRAUNQUENTIN C PFEIFFER RA SCHINZEL A
Citation: D. Kotzot et al., ISOCHROMOSOME 18P RESULTS FROM MATERNAL MEIOSIS-II NONDISJUNCTION, European journal of human genetics, 4(3), 1996, pp. 168-174
PRENATAL-DIAGNOSIS OF BETA-THALASSEMIA AND SICKLE-CELL-ANEMIA IN TURKEY
Authors: TUZMEN S TADMOURI GO OZER A BAIG SM OZCELIK H BASARAN S BASAK AN
Citation: S. Tuzmen et al., PRENATAL-DIAGNOSIS OF BETA-THALASSEMIA AND SICKLE-CELL-ANEMIA IN TURKEY, Prenatal diagnosis, 16(3), 1996, pp. 252-258
CLINICAL AND CYTOGENETIC STUDIES OF 2 CASES OF KLINEFELTER SYNDROME WITH HEREDITARY RETINOBLASTOMA AND RHABDOMYOSARCOMA
Authors: OGUR G SENGUN Z ARELKILIC G DEBUSSCHER C BASARAN S OZBEK U AYAN I SARIBAN E VAMOS E
Citation: G. Ogur et al., CLINICAL AND CYTOGENETIC STUDIES OF 2 CASES OF KLINEFELTER SYNDROME WITH HEREDITARY RETINOBLASTOMA AND RHABDOMYOSARCOMA, Cancer genetics and cytogenetics, 89(1), 1996, pp. 77-81
PARENTAL ORIGIN OF THE EXTRA HAPLOID CHROMOSOME SET IN TRIPLOIDIES DIAGNOSED PRENATALLY
Authors: MINY P KOPPERS B DWORNICZAK B BOGDANOVA N HOLZGREVE W TERCANLI S BASARAN S REHDER H EXELER R HORST J
Citation: P. Miny et al., PARENTAL ORIGIN OF THE EXTRA HAPLOID CHROMOSOME SET IN TRIPLOIDIES DIAGNOSED PRENATALLY, American journal of medical genetics, 57(1), 1995, pp. 102-106
TETRA-AMELIA, LUNG HYPO- APLASIA, CLEFT LIP-PALATE, AND HEART DEFECT - A NEW SYNDROME/
Authors: BASARAN S YUKSEL A ERMIS H KUSEYRI F AGAN M YUKSELAPAK M
Citation: S. Basaran et al., TETRA-AMELIA, LUNG HYPO- APLASIA, CLEFT LIP-PALATE, AND HEART DEFECT - A NEW SYNDROME/, American journal of medical genetics, 51(1), 1994, pp. 77-80
MULTIPLE ORIGINS OF X-CHROMOSOME TETRASOMY
Authors: ROBINSON W BINKERT F SCHINZEL A BASARAN S MIKELSAAR R
Citation: W. Robinson et al., MULTIPLE ORIGINS OF X-CHROMOSOME TETRASOMY, Journal of Medical Genetics, 31(5), 1994, pp. 424-425
A SOMATIC ORIGIN OF HOMOLOGOUS ROBERTSONIAN TRANSLOCATIONS AND ISOCHROMOSOMES
Authors: ROBINSON WP BERNASCONI F BASARAN S YUKSELAPAK M NERI G SERVILLE F BALICEK P HALUZA R FARAH LMS LULECI G SCHINZEL AA
Citation: Wp. Robinson et al., A SOMATIC ORIGIN OF HOMOLOGOUS ROBERTSONIAN TRANSLOCATIONS AND ISOCHROMOSOMES, American journal of human genetics, 54(2), 1994, pp. 290-302
MATERNAL UNIPARENTAL DISOMY-22 HAS NO IMPACT ON THE PHENOTYPE
Authors: SCHINZEL AA BASARAN S BERNASCONI F KARAMAN B YUKSELAPAK M ROBINSON WP
Citation: Aa. Schinzel et al., MATERNAL UNIPARENTAL DISOMY-22 HAS NO IMPACT ON THE PHENOTYPE, American journal of human genetics, 54(1), 1994, pp. 21-24
ROBERTSONIAN TRANSLOCATIONS BETWEEN HOMOLOGOUS CHROMOSOMES ARE SOMATIC EVENTS
Authors: ROBINSON WP BERNASCONI F BLOUIN JL BASARAN S NERI G ZIZKA J ANTONARAKIS SE SCHINZEL AA
Citation: Wp. Robinson et al., ROBERTSONIAN TRANSLOCATIONS BETWEEN HOMOLOGOUS CHROMOSOMES ARE SOMATIC EVENTS, American journal of human genetics, 53(3), 1993, pp. 121-121
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