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Results: 1-25 | 26-28
Results: 1-25/28
SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME
Authors: SILLEN A ANTONLAMPRECHT I BRAUNQUENTIN C KRAUS CS SAYLI BS AYUSO C JAGELL S KUSTER W WADELIUS C
Citation: A. Sillen et al., SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME, Human mutation, 12(6), 1998, pp. 377-384
AN ASSESSMENT OF FERTILITY IN BORON-EXPOSED TURKISH SUBPOPULATIONS
Authors: SAYLI BS TUCCAR E ELHAN AH
Citation: Bs. Sayli et al., AN ASSESSMENT OF FERTILITY IN BORON-EXPOSED TURKISH SUBPOPULATIONS, Reproductive toxicology, 12(3), 1998, pp. 297-304
ANTIOXIDATIVE METABOLISM IN DOWN-SYNDROME
Authors: TEKSEN F SAYLI BS AYDIN A SAYAL A ISIMER A
Citation: F. Teksen et al., ANTIOXIDATIVE METABOLISM IN DOWN-SYNDROME, Biological trace element research, 63(2), 1998, pp. 123-127
MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W DEBOULLE K HENDRICKX J BAKKER E VANHOENACKER F MOLLICA F LUDECKE HJ SAYLI BS PAZZAGLIA UE MORTIER G HAMEL B CONRAD EU MATSUSHITA M RASKIND WH WILLEMS PJ
Citation: W. Wuyts et al., MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES, American journal of human genetics, 62(2), 1998, pp. 346-354
SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME
Authors: SILLEN A KRAUS CS ANTONLAMBRECHT I JAGELL S KUSTER W SAYLI BS AYUSO C WADELIUS C
Citation: A. Sillen et al., SPECTRUM OF MUTATIONS AND SEQUENCE VARIANTS IN THE FALDH GENE IN PATIENTS WITH SJOGREN-LARSSON-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 2029-2029
A 2ND LOCUS (GLC3B) FOR PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) MAPS TO THE 1P36 REGION
Authors: AKARSU AN TURACLI ME AKTAN SG BARSOUMHOMSY M CHEVRETTE L SAYLI BS SARFARAZI M
Citation: An. Akarsu et al., A 2ND LOCUS (GLC3B) FOR PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) MAPS TO THE 1P36 REGION, Human molecular genetics, 5(8), 1996, pp. 1199-1203
GENOMIC STRUCTURE OF HOXD13 GENE - A 9-POLYALANINE DUPLICATION CAUSESSYNPOLYDACTYLY IN 2 UNRELATED FAMILIES
Authors: AKARSU AN STOILOV I YILMAZ E SAYLI BS SARFARAZI M
Citation: An. Akarsu et al., GENOMIC STRUCTURE OF HOXD13 GENE - A 9-POLYALANINE DUPLICATION CAUSESSYNPOLYDACTYLY IN 2 UNRELATED FAMILIES, Human molecular genetics, 5(7), 1996, pp. 945-952
FINE MAPPING OF THE SYNPOLYDACTYLY LOCUS ON THE 2Q31 REGION
Authors: AKARSU AN SAYLI BS SARFARAZI M
Citation: An. Akarsu et al., FINE MAPPING OF THE SYNPOLYDACTYLY LOCUS ON THE 2Q31 REGION, Cytogenetics and cell genetics, 73(4), 1996, pp. 11-11
GENETIC-LINKAGE OF PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) TO CHROMOSOME 2P21 AND PHYSICAL MAPPING OF THE CANDIDATE REGION
Authors: STOILOV I AKARSU AN HOSSAIN A TURACLI ME AKTAN SG BARSOUMHOMSY M CHEVRETTE L SAYLI BS SARFARAZI M
Citation: I. Stoilov et al., GENETIC-LINKAGE OF PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) TO CHROMOSOME 2P21 AND PHYSICAL MAPPING OF THE CANDIDATE REGION, Cytogenetics and cell genetics, 73(4), 1996, pp. 12-12
EXCLUSION OF PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) FROM 2 CANDIDATE REGIONS OF CHROMOSOME ARM 6P AND CHROMOSOME-11 (VOL 61, PG 290, 1996)
Authors: AKARSU AN TURACLI ME AKTAN SG HOSSAIN A BARSOUMHOMSY M CHEVRETTE L SAYLI BS SARFARAZI M
Citation: An. Akarsu et al., EXCLUSION OF PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) FROM 2 CANDIDATE REGIONS OF CHROMOSOME ARM 6P AND CHROMOSOME-11 (VOL 61, PG 290, 1996), American journal of medical genetics, 62(1), 1996, pp. 102-102
EXCLUSION OF PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) FROM 2 CANDIDATE REGIONS OF CHROMOSOME ARM 6P AND CHROMOSOME-11
Authors: AKARSU AN TURACLI ME AKTAN SG HOSSAIN A BARSOUMHOMSY M CHEVRETTE L SAYLI BS SARFARAZI M
Citation: An. Akarsu et al., EXCLUSION OF PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) FROM 2 CANDIDATE REGIONS OF CHROMOSOME ARM 6P AND CHROMOSOME-11, American journal of medical genetics, 61(3), 1996, pp. 290-292
ANTISPERM ANTIBODY AND KLINEFELTER SYNDROME - DOES AUTOIMMUNITY PLAY A ROLE IN THE PATHOGENESIS
Authors: SENGUL A GUL D SAYLI BS HACIBEKTASOGLU A
Citation: A. Sengul et al., ANTISPERM ANTIBODY AND KLINEFELTER SYNDROME - DOES AUTOIMMUNITY PLAY A ROLE IN THE PATHOGENESIS, Urologia internationalis, 57(2), 1996, pp. 77-79
LOCALIZATION OF THE SYNDACTYLY TYPE-II (SYNPOLYDACTYLY) LOCUS TO 2Q31REGION AND IDENTIFICATION OF TIGHT LINKAGE TO HOXD8 INTRAGENIC MARKER
Authors: SARFARAZI M AKARSU AN SAYLI BS
Citation: M. Sarfarazi et al., LOCALIZATION OF THE SYNDACTYLY TYPE-II (SYNPOLYDACTYLY) LOCUS TO 2Q31REGION AND IDENTIFICATION OF TIGHT LINKAGE TO HOXD8 INTRAGENIC MARKER, Human molecular genetics, 4(8), 1995, pp. 1453-1458
ASSIGNMENT OF A LOCUS (GLC3A) FOR PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) TO 2P21 AND EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: SARFARAZI M AKARSU AN HOSSAIN A TURACLI ME AKTAN SG BARSOUMHOMSY M CHEVRETTE L SAYLI BS
Citation: M. Sarfarazi et al., ASSIGNMENT OF A LOCUS (GLC3A) FOR PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS) TO 2P21 AND EVIDENCE FOR GENETIC-HETEROGENEITY, Genomics, 30(2), 1995, pp. 171-177
CONFINED PLACENTAL MOSAICISM IN TERM PLACENTAE - ANALYSIS OF 125 CASES
Authors: ARTAN S BASARAN N HASSA H OZALP S SENER T SAYLI BS CENGIZ C OZDEMIR M DURAK T DOLEN I OZGUNEN T TUNA M
Citation: S. Artan et al., CONFINED PLACENTAL MOSAICISM IN TERM PLACENTAE - ANALYSIS OF 125 CASES, Prenatal diagnosis, 15(12), 1995, pp. 1135-1142
SISTER-CHROMATID EXCHANGE ANALYSIS IN ACUTE-LEUKEMIA PATIENTS
Authors: TUNA M ARTAN S GEZER S SAYLI BS BASARAN N
Citation: M. Tuna et al., SISTER-CHROMATID EXCHANGE ANALYSIS IN ACUTE-LEUKEMIA PATIENTS, Cancer genetics and cytogenetics, 79(1), 1995, pp. 86-88
ANOPHTHALMOS-SYNDACTYLY (WAARDENBURG) SYNDROME WITHOUT OLIGODACTYLY OF TOES
Authors: SAYLI BS AKARSU AN ALTAN S
Citation: Bs. Sayli et al., ANOPHTHALMOS-SYNDACTYLY (WAARDENBURG) SYNDROME WITHOUT OLIGODACTYLY OF TOES, American journal of medical genetics, 58(1), 1995, pp. 18-20
A LARGE TURKISH KINDRED WITH SYNDACTYLY TYPE-II (SYNPOLYDACTYLY) .1. FIELD INVESTIGATION, CLINICAL AND PEDIGREE DATA
Authors: SAYLI BS AKARSU AN SAYLI U AKHAN O CEYLANER S SARFARAZI M
Citation: Bs. Sayli et al., A LARGE TURKISH KINDRED WITH SYNDACTYLY TYPE-II (SYNPOLYDACTYLY) .1. FIELD INVESTIGATION, CLINICAL AND PEDIGREE DATA, Journal of Medical Genetics, 32(6), 1995, pp. 421-434
A LARGE TURKISH KINDRED WITH SYNDACTYLY TYPE-II (SYNPOLYDACTYLY) .2. HOMOZYGOUS PHENOTYPE
Authors: AKARSU AN AKHAN O SAYLI BS SAYLI U BASKAYA G SARFARAZI M
Citation: An. Akarsu et al., A LARGE TURKISH KINDRED WITH SYNDACTYLY TYPE-II (SYNPOLYDACTYLY) .2. HOMOZYGOUS PHENOTYPE, Journal of Medical Genetics, 32(6), 1995, pp. 435-441
GENETIC FEATURES OF RETINITIS-PIGMENTOSA IN TURKEY
Authors: ATMACA LS SAYLI BS AKARSU N GUNDUZ K
Citation: Ls. Atmaca et al., GENETIC FEATURES OF RETINITIS-PIGMENTOSA IN TURKEY, Documenta ophthalmologica, 89(4), 1995, pp. 387-392
LOCALIZATION OF THE SYNPOLYDACTYL LOCUS TO 2Q31 REGION AND IDENTIFICATION OF TIGHT LINKAGE TO THE HOXD GENE-CLUSTER
Authors: SARFARAZI M AKARSU AN SAYLI BS
Citation: M. Sarfarazi et al., LOCALIZATION OF THE SYNPOLYDACTYL LOCUS TO 2Q31 REGION AND IDENTIFICATION OF TIGHT LINKAGE TO THE HOXD GENE-CLUSTER, American journal of human genetics, 57(4), 1995, pp. 1164-1164
PHENOTYPE-GENOTYPE CORRELATION OF 7 HOMOZYGOTE INDIVIDUALS IN A LARGEKINDRED WITH SYNPOLYDACTYLY
Authors: AKARSU AN STOILOV I SAYLI BS SARFARAZI M
Citation: An. Akarsu et al., PHENOTYPE-GENOTYPE CORRELATION OF 7 HOMOZYGOTE INDIVIDUALS IN A LARGEKINDRED WITH SYNPOLYDACTYLY, American journal of human genetics, 57(4), 1995, pp. 1352-1352
EXCLUSION MAPPING OR AUTOSOMAL RECESSIVE PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS)
Authors: HOSSAIN A AKARSU AN TURACLI ME AKTAN SG BARSOUMHOMSY M CHEVRETTE L SAYLI BS SARFARAZI M
Citation: A. Hossain et al., EXCLUSION MAPPING OR AUTOSOMAL RECESSIVE PRIMARY CONGENITAL GLAUCOMA (BUPHTHALMOS), American journal of human genetics, 57(4), 1995, pp. 1879-1879
KLINEFELTER SYNDROME-ASSOCIATED WITH 13 14 TRANSLOCATION ABNORMALITY 46,XXY,T(13Q14Q)/
Authors: GUL D SAYLI BS
Citation: D. Gul et Bs. Sayli, KLINEFELTER SYNDROME-ASSOCIATED WITH 13 14 TRANSLOCATION ABNORMALITY 46,XXY,T(13Q14Q)/, Urologia internationalis, 52(3), 1994, pp. 166-168
EFFECTS OF CONSANGUINITY ON ANTHROPOMETRIC MEASUREMENTS OF NEWBORN-INFANTS
Authors: BASARAN N ARTAN S YAZICIOGLU S SAYLI BS
Citation: N. Basaran et al., EFFECTS OF CONSANGUINITY ON ANTHROPOMETRIC MEASUREMENTS OF NEWBORN-INFANTS, Clinical genetics, 45(4), 1994, pp. 208-211
Risultati: 1-25 | 26-28