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Results: 1-19 |
Results: 19
GRANULOCYTIC SARCOMA IN THE DIFFERENTIAL-DIAGNOSIS OF SMALL ROUND-CELL TUMOR OF CHILDHOOD - A CASE-REPORT
Authors: AYAN I KEBUDI R OGUR G TUZUNER N DOGAN O
Citation: I. Ayan et al., GRANULOCYTIC SARCOMA IN THE DIFFERENTIAL-DIAGNOSIS OF SMALL ROUND-CELL TUMOR OF CHILDHOOD - A CASE-REPORT, International journal of pediatric hematology/oncology, 5(1), 1998, pp. 29-34
ASSESSMENT OF PYRIN GENE-MUTATIONS IN TURKS WITH FAMILIAL MEDITERRANEAN FEVER (FMF)
Authors: CHEN XG FISCHELGHODSIAN N CERCEK A HAMON M OGUR G LOTAN R DANON Y SHOHAT M
Citation: Xg. Chen et al., ASSESSMENT OF PYRIN GENE-MUTATIONS IN TURKS WITH FAMILIAL MEDITERRANEAN FEVER (FMF), Human mutation, 11(6), 1998, pp. 456-460
THE DELTA-CCR5 MUTATION CONFERRING PROTECTION AGAINST HIV-1 IN CAUCASIAN POPULATIONS HAS A SINGLE AND RECENT ORIGIN IN NORTHEASTERN EUROPE
Authors: LIBERT F COCHAUX P BECKMAN G SAMSON M AKSENOVA M CAO A CZEIZEL A CLAUSTRES M DELARUA C FERRARI M FERREC C GLOVER G GRINDE B GURAN S KUCINSKAS V LAVINHA J MERCIER B OGUR G PELTONEN L ROSATELLI C SCHWARTZ M SPITSYN V TIMAR L BECKMAN L PARMENTIER M VASSART G
Citation: F. Libert et al., THE DELTA-CCR5 MUTATION CONFERRING PROTECTION AGAINST HIV-1 IN CAUCASIAN POPULATIONS HAS A SINGLE AND RECENT ORIGIN IN NORTHEASTERN EUROPE, Human molecular genetics, 7(3), 1998, pp. 399-406
DEL(17)(Q25) IN A PATIENT WITH HAIRY-CELL LEUKEMIA - A NEW CLONAL CHROMOSOME ABNORMALITY
Authors: SUCAK GT OGUR G TOPAL G ATAOGLU O CANKUS G HAZNEDAR R
Citation: Gt. Sucak et al., DEL(17)(Q25) IN A PATIENT WITH HAIRY-CELL LEUKEMIA - A NEW CLONAL CHROMOSOME ABNORMALITY, Cancer genetics and cytogenetics, 100(2), 1998, pp. 152-154
CYTOGENETIC ANALYSIS OF 40 SPONTANEOUS-ABORTIONS THROUGH CHORIONIC VILLI
Authors: BAHCE M IMIRZALIOGLU N CANKUS G TUNCA Y DURAK T OZEN S GUL D OGUR G
Citation: M. Bahce et al., CYTOGENETIC ANALYSIS OF 40 SPONTANEOUS-ABORTIONS THROUGH CHORIONIC VILLI, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 91-91
DETECTION OF FETAL CRI-DU-CHAT SYNDROME WITH MULTIPLE MARKER SCREENING - IS IT JUST A COINCIDENCE
Authors: OGUR G ONDEROGLU L DURAN E GURAN S BAHGE M
Citation: G. Ogur et al., DETECTION OF FETAL CRI-DU-CHAT SYNDROME WITH MULTIPLE MARKER SCREENING - IS IT JUST A COINCIDENCE, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 170-170
ASSOCIATION A CONGENITAL LEUKEMIA, DOWN-SYNDROME AND BILATERAL SYNDACTYLY IN A NEWBORN MALE
Authors: OGUR G OZCAN O GUL D BAHCE M GURAN S ERDEM G TUNCA Y DURAK T OZEN S IMIRZALIOGLU N
Citation: G. Ogur et al., ASSOCIATION A CONGENITAL LEUKEMIA, DOWN-SYNDROME AND BILATERAL SYNDACTYLY IN A NEWBORN MALE, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 258-258
DETECTION OF FETAL CRI-DU-CHAT SYNDROME WITH MULTIPLE MARKER SCREENING - IS IT JUST A COINCIDENCE
Authors: OGUR G ONDEROGLU LS DURAN EH GURAN S BAHCE M
Citation: G. Ogur et al., DETECTION OF FETAL CRI-DU-CHAT SYNDROME WITH MULTIPLE MARKER SCREENING - IS IT JUST A COINCIDENCE, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 259-259
DIAGNOSTIC AND PROGNOSTIC IMPLICATIONS OF CYTOGENETIC STUDIES IN LEUKEMIAS - RESULTS OF 28 CASES
Authors: OGUR G SUCAK G HAZNEDAROGLU R CANKUS G BAHCE H YAVUZ G
Citation: G. Ogur et al., DIAGNOSTIC AND PROGNOSTIC IMPLICATIONS OF CYTOGENETIC STUDIES IN LEUKEMIAS - RESULTS OF 28 CASES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 334-334
APPLICATION OF THE APT TEST IN PRENATAL-DIAGNOSIS TO EVALUATE THE FETAL ORIGIN OF BLOOD OBTAINED BY CORDOCENTESIS - RESULTS OF 30 PREGNANCIES
Authors: OGUR G GUL D OZEN S IMIRZALIOGLU N CANKUS G TUNCA Y BAHCE M GURAN S BASER I
Citation: G. Ogur et al., APPLICATION OF THE APT TEST IN PRENATAL-DIAGNOSIS TO EVALUATE THE FETAL ORIGIN OF BLOOD OBTAINED BY CORDOCENTESIS - RESULTS OF 30 PREGNANCIES, Prenatal diagnosis, 17(9), 1997, pp. 879-882
AMYLOIDOSIS IN FMF IS ASSOCIATED WITH A SPECIFIC CORE HAPLOTYPE IN THE MEFV LOCUS
Authors: SHOHAT M LOTAN R MAGAL N OGUR G TOKGUZ G SCHWABE A FISCHELGHODSIAN N KASTNER D ROTTER JI SCHLEZINGER M DANON Y
Citation: M. Shohat et al., AMYLOIDOSIS IN FMF IS ASSOCIATED WITH A SPECIFIC CORE HAPLOTYPE IN THE MEFV LOCUS, American journal of human genetics, 61(4), 1997, pp. 258-258
THE VARIOUS FMF CORE HAPLOTYPES IN THE MEFV LOCUS AND THEIR CORRELATION WITH FMF SYMPTOMS
Authors: DAGAN T LOTAN R DANON Y MAGAL N OGUR G TOKGUZ G SCHWABE A FISCHELGHODSIAN N ROTTER JI SCHLEZINGER M HALPERN GJ SHOHAT M
Citation: T. Dagan et al., THE VARIOUS FMF CORE HAPLOTYPES IN THE MEFV LOCUS AND THEIR CORRELATION WITH FMF SYMPTOMS, American journal of human genetics, 61(4), 1997, pp. 1136-1136
FINE MAPPING OF THE SPLIT HAND-SPLIT FOOT (SHFM3) LOCUS AT 10Q24 - EVIDENCE FOR ANTICIPATION AND SEGREGATION DISTORTION
Authors: OZEN RS BAYSAL BE FAN JE DEVLIN B GORRY M EHRLICH G OGUR G RICHARD CW
Citation: Rs. Ozen et al., FINE MAPPING OF THE SPLIT HAND-SPLIT FOOT (SHFM3) LOCUS AT 10Q24 - EVIDENCE FOR ANTICIPATION AND SEGREGATION DISTORTION, American journal of human genetics, 61(4), 1997, pp. 1689-1689
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
A NEW DELETION OF THE 5-ALPHA-REDUCTASE TYPE-2 GENE IN A TURKISH FAMILY WITH 5-ALPHA-REDUCTASE DEFICIENCY
Authors: BOUDON C LOBACCARO JM LUMBROSO S OGUR G OCAL G BELON C SULTAN C
Citation: C. Boudon et al., A NEW DELETION OF THE 5-ALPHA-REDUCTASE TYPE-2 GENE IN A TURKISH FAMILY WITH 5-ALPHA-REDUCTASE DEFICIENCY, Clinical endocrinology, 43(2), 1995, pp. 183-188
PRENATAL-DIAGNOSIS OF AUTOSOMAL RECESSIVE OSTEOPETROSIS, INFANTILE TYPE, BY X-RAY EVALUATION
Authors: OGUR G OGUR E CELASUN B BASER I IMIRZALIOGLU N OZTURK T ALEMDAROGLU A
Citation: G. Ogur et al., PRENATAL-DIAGNOSIS OF AUTOSOMAL RECESSIVE OSTEOPETROSIS, INFANTILE TYPE, BY X-RAY EVALUATION, Prenatal diagnosis, 15(5), 1995, pp. 477-481
MULTIPLE CLONAL CHROMOSOME-ABERRATIONS IN A CASE OF CHILDHOOD FOCAL NODULAR HYPERPLASIA OF THE LIVER
Authors: HEIMANN P OGUR G DEBUSSCHER C DEVALCK C SARIBAN E DEPREZ C DEROY G VAMOS E
Citation: P. Heimann et al., MULTIPLE CLONAL CHROMOSOME-ABERRATIONS IN A CASE OF CHILDHOOD FOCAL NODULAR HYPERPLASIA OF THE LIVER, Cancer genetics and cytogenetics, 85(2), 1995, pp. 138-142
CLINICAL, ULTRASTRUCTURAL AND BIOCHEMICAL-STUDIES IN 2 SIBS WITH EHLERS-DANLOS-SYNDROME TYPE-VI-B-LIKE FEATURES
Authors: OGUR G BAYKAN N DEPAEPE A STEINMANN B QUATACKER J KUSEYRI F YUKSELAPAK M
Citation: G. Ogur et al., CLINICAL, ULTRASTRUCTURAL AND BIOCHEMICAL-STUDIES IN 2 SIBS WITH EHLERS-DANLOS-SYNDROME TYPE-VI-B-LIKE FEATURES, Clinical genetics, 46(6), 1994, pp. 417-422
CHROMOSOMAL FINDINGS IN CULTURED MELANOCYTES FROM A GIANT CONGENITAL NEVUS
Authors: HEIMANN P OGUR G DEBUSSCHER C MORANDINI R LIBERT A VAMOS E
Citation: P. Heimann et al., CHROMOSOMAL FINDINGS IN CULTURED MELANOCYTES FROM A GIANT CONGENITAL NEVUS, Cancer genetics and cytogenetics, 68(1), 1993, pp. 74-77
Risultati: 1-19 |