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Results: 1-12 |
Results: 12
A NEW MULTIPLE CONGENITAL ANOMALY, MENTAL-RETARDATION SYNDROME WITH PREAXIAL BRACHYDACTYLY, HYPERPHALANGISM, DEAFNESS AND ORODENTAL ANOMALIES
Authors: TEMTAMY SA MEGUID NA ISMAIL SI RAMZY MI
Citation: Sa. Temtamy et al., A NEW MULTIPLE CONGENITAL ANOMALY, MENTAL-RETARDATION SYNDROME WITH PREAXIAL BRACHYDACTYLY, HYPERPHALANGISM, DEAFNESS AND ORODENTAL ANOMALIES, Clinical dysmorphology, 7(4), 1998, pp. 249-255
BETA-GLOBIN GENE HAPLOTYPES IN EGYPTIAN SICKLE-CELL DISEASE AND BETA-THALASSEMIA (VOL 18, PG 587, 1997)
Authors: ELHAZMI MAF WARSY AS HUSSEIN IMR ELBESHLAWY AMI TEMTAMY SA
Citation: Maf. Elhazmi et al., BETA-GLOBIN GENE HAPLOTYPES IN EGYPTIAN SICKLE-CELL DISEASE AND BETA-THALASSEMIA (VOL 18, PG 587, 1997), Saudi medical journal, 19(4), 1998, pp. 531-531
BETA-GLOBIN GENE HAPLOTYPES IN EGYPTIAN SICKLE-CELL DISEASE AND BETA-THALASSEMIA
Authors: ELHAZMI MAF WARSY AS HUSSEIN IMR ELBESHLAWY AMI TEMTAMY SA
Citation: Maf. Elhazmi et al., BETA-GLOBIN GENE HAPLOTYPES IN EGYPTIAN SICKLE-CELL DISEASE AND BETA-THALASSEMIA, Saudi medical journal, 18(6), 1997, pp. 587-590
IDENTIFICATION OF MEDITERRANEAN BETA-THALASSEMIA MUTATIONS BY REVERSEDOT-BLOT IN ITALIANS AND EGYPTIANS
Authors: RADY MS BAFFICO M KHALIFA AS HESHMAT NM ELMOSELHY S SCIARRATTA GV HUSSEIN IR TEMTAMY SA ROMEO G
Citation: Ms. Rady et al., IDENTIFICATION OF MEDITERRANEAN BETA-THALASSEMIA MUTATIONS BY REVERSEDOT-BLOT IN ITALIANS AND EGYPTIANS, Hemoglobin, 21(1), 1997, pp. 59-69
MOLECULAR ANALYSIS OF ANDROGEN RESISTANCE SYNDROMES IN EGYPTIAN PATIENTS
Authors: ESSAWI M GAD YZ ELROUBY O TEMTAMY SA SABOUR YA ELAWADY MK
Citation: M. Essawi et al., MOLECULAR ANALYSIS OF ANDROGEN RESISTANCE SYNDROMES IN EGYPTIAN PATIENTS, Disease markers, 13(2), 1997, pp. 99-105
GAPO-SYNDROME - FIRST EGYPTIAN CASE WITH ULTRASTRUCTURAL-CHANGES IN THE GINGIVA
Authors: MEGUID NA AFIFI HH RAMZY MI HINDAWY A TEMTAMY SA
Citation: Na. Meguid et al., GAPO-SYNDROME - FIRST EGYPTIAN CASE WITH ULTRASTRUCTURAL-CHANGES IN THE GINGIVA, Clinical genetics, 52(2), 1997, pp. 110-115
NEW AUTOSOMAL RECESSIVE MULTIPLE CONGENITAL-ABNORMALITIES MENTAL-RETARDATION SYNDROME WITH CRANIOFACIAL DYSMORPHISM ABSENT CORPUS-CALLOSUM,IRIS COLOBOMAS AND CONNECTIVE-TISSUE DYSPLASIA
Authors: TEMTAMY SA SALAM MA ABOULEZZ EHA HUSSEIN HA HELMY SAH SHALASH BA
Citation: Sa. Temtamy et al., NEW AUTOSOMAL RECESSIVE MULTIPLE CONGENITAL-ABNORMALITIES MENTAL-RETARDATION SYNDROME WITH CRANIOFACIAL DYSMORPHISM ABSENT CORPUS-CALLOSUM,IRIS COLOBOMAS AND CONNECTIVE-TISSUE DYSPLASIA, Clinical dysmorphology, 5(3), 1996, pp. 231-240
GREIG CEPHALOPOLYSYNDACTYLY SYNDROME WITH DYSGENESIS OF THE CORPUS-CALLOSUM IN A BEDOUIN FAMILY
Authors: MARAFIE MJ TEMTAMY SA RAJARAM U ALAWADI SA ELBADRAMANY MH FARAG TI
Citation: Mj. Marafie et al., GREIG CEPHALOPOLYSYNDACTYLY SYNDROME WITH DYSGENESIS OF THE CORPUS-CALLOSUM IN A BEDOUIN FAMILY, American journal of medical genetics, 66(3), 1996, pp. 261-264
COFS SYNDROME WITH FAMILIAL 1-16-TRANSLOCATION
Authors: TEMTAMY SA MEGUID NA MAHMOUD A AFIFI HH GERZAWY A ZAKI MS
Citation: Sa. Temtamy et al., COFS SYNDROME WITH FAMILIAL 1-16-TRANSLOCATION, Clinical genetics, 50(4), 1996, pp. 240-243
AN EPIDEMIOLOGIC GENETIC-STUDY OF MENTAL-SUBNORMALITY IN ASSIUT-GOVERNORATE, EGYPT
Authors: TEMTAMY SA KANDIL MR DEMERDASH AM HASSAN WA MEGUID NA AFIFI HH
Citation: Sa. Temtamy et al., AN EPIDEMIOLOGIC GENETIC-STUDY OF MENTAL-SUBNORMALITY IN ASSIUT-GOVERNORATE, EGYPT, Clinical genetics, 46(5), 1994, pp. 347-351
MOLECULAR CHARACTERIZATION OF BETA-THALASSEMIA IN EGYPTIANS
Authors: HUSSEIN IR TEMTAMY SA ELBESHLAWY A FEARON C SHALABY Z VASSILOPOULOS G KAZAZIAN HH
Citation: Ir. Hussein et al., MOLECULAR CHARACTERIZATION OF BETA-THALASSEMIA IN EGYPTIANS, Human mutation, 2(1), 1993, pp. 48-52
KARYOTYPE PHENOTYPE CORRELATION IN FEMALES WITH SHORT STATURE
Authors: TEMTAMY SA GHALI I SALAM MA HUSSEIN FH EZZ EHAA SALAH N
Citation: Sa. Temtamy et al., KARYOTYPE PHENOTYPE CORRELATION IN FEMALES WITH SHORT STATURE, Clinical genetics, 41(3), 1992, pp. 147-151
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