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Results: 1-25 | 26-37
Results: 1-25/37
THE AUTOSOMAL RECESSIVE CONGENITAL INTRAUTERINE INFECTION-LIKE SYNDROME OF MICROCEPHALY, INTRACRANIAL CALCIFICATION, AND CNS DISEASE - REPORT OF ANOTHER BEDOUIN FAMILY
Authors: ALDABBOUS R SABRY MA FARAH S ALAWADI SA SIMEONOV S FARAG TI
Citation: R. Aldabbous et al., THE AUTOSOMAL RECESSIVE CONGENITAL INTRAUTERINE INFECTION-LIKE SYNDROME OF MICROCEPHALY, INTRACRANIAL CALCIFICATION, AND CNS DISEASE - REPORT OF ANOTHER BEDOUIN FAMILY, Clinical dysmorphology, 7(2), 1998, pp. 127-130
LISSENCEPHALY REVISITED
Authors: SABRY MA FARAH SA FARAG TI
Citation: Ma. Sabry et al., LISSENCEPHALY REVISITED, Journal of the American Academy of Child and Adolescent Psychiatry, 37(9), 1998, pp. 899-899
TRIOPHTHALMIA AND FACIAL CLEFTING - A CASE-REPORT
Authors: TAYEL SM SABRY MA ABDELKADER N FARAH S ALAWADI SA FARAG TI
Citation: Sm. Tayel et al., TRIOPHTHALMIA AND FACIAL CLEFTING - A CASE-REPORT, Journal of Medical Genetics, 35(10), 1998, pp. 875-877
ETIOLOGY OF RECURRENCE OF ANEUPLOIDY TRISOMY-21 IN SIBLINGS/
Authors: MURTHY DSK FARAG TI
Citation: Dsk. Murthy et Ti. Farag, ETIOLOGY OF RECURRENCE OF ANEUPLOIDY TRISOMY-21 IN SIBLINGS/, Cytogenetics and cell genetics, 77, 1997, pp. 7-7
CYTOGENETIC PROFILE OF DOWN-SYNDROME IN KUWAIT
Authors: ALAWADI SA MURTHY DSK FARAG TI
Citation: Sa. Alawadi et al., CYTOGENETIC PROFILE OF DOWN-SYNDROME IN KUWAIT, Cytogenetics and cell genetics, 77, 1997, pp. 7-7
KENNY-CAFFEY-SYNDROME IN 6 BEDOUIN SIBSHIPS - AUTOSOMAL RECESSIVE INHERITANCE IS CONFIRMED
Authors: KHAN KTS UMA R USHA R ALGHANEM MM ALAWADI SA FARAG TI
Citation: Kts. Khan et al., KENNY-CAFFEY-SYNDROME IN 6 BEDOUIN SIBSHIPS - AUTOSOMAL RECESSIVE INHERITANCE IS CONFIRMED, American journal of medical genetics, 69(2), 1997, pp. 126-132
ANOTHER ARAB PATIENT WITH OVERLAP OF VARADI-PAPP OPITZ TRIGONOCEPHALYSYNDROMES/
Authors: SABRY MA ALSALEH Q FARAH S OBENBERGEROVA D SIMEONOV S ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., ANOTHER ARAB PATIENT WITH OVERLAP OF VARADI-PAPP OPITZ TRIGONOCEPHALYSYNDROMES/, American journal of medical genetics, 68(1), 1997, pp. 54-57
LISSENCEPHALY ASSOCIATED WITH CEREBELLAR HYPOPLASIA AND MYOCLONIC EPILEPSY IN A BEDOUIN KINDRED - A NEW SYNDROME
Authors: FARAH S SABRY MA KHURAIBET A KHAFFAGI S RUDWAN M HASSAN M HASEEB N ABULHASSAN S ABDELRASOOL MA ELGAMAL S QASRAWI B ALBUSAIRI W FARAG TI
Citation: S. Farah et al., LISSENCEPHALY ASSOCIATED WITH CEREBELLAR HYPOPLASIA AND MYOCLONIC EPILEPSY IN A BEDOUIN KINDRED - A NEW SYNDROME, Clinical genetics, 51(5), 1997, pp. 326-330
PERICENTRIC-INVERSION OF CHROMOSOME-1 AND CHROMOSOME-9 [46,XY,INV(1)(P12-Q13), INV(9)(P11-Q12), 16QH+] IN A MALE WITH REPRODUCTIVE FAILURE
Authors: MURTHY DSK FARAG TI ALAWADI SA
Citation: Dsk. Murthy et al., PERICENTRIC-INVERSION OF CHROMOSOME-1 AND CHROMOSOME-9 [46,XY,INV(1)(P12-Q13), INV(9)(P11-Q12), 16QH+] IN A MALE WITH REPRODUCTIVE FAILURE, American journal of human genetics, 61(4), 1997, pp. 2182-2182
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
HAND ANOMALIES IN FETAL-HYDANTOIN SYNDROME - FROM NAIL PHALANGEAL HYPOPLASIA TO UNILATERAL ACHEIRIA
Authors: SABRY MA FARAG TI
Citation: Ma. Sabry et Ti. Farag, HAND ANOMALIES IN FETAL-HYDANTOIN SYNDROME - FROM NAIL PHALANGEAL HYPOPLASIA TO UNILATERAL ACHEIRIA, American journal of medical genetics, 62(4), 1996, pp. 410-412
FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME WITH BIFID HALLUX, ABSENT TIBIA, AND MACROPHALLUS - A REPORT OF A BEDOUIN BABY
Authors: SABRY MA OBENBERGEROVA D ALSAWAN R ALSALEH Q FARAH S ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME WITH BIFID HALLUX, ABSENT TIBIA, AND MACROPHALLUS - A REPORT OF A BEDOUIN BABY, Journal of Medical Genetics, 33(2), 1996, pp. 165-167
INDIRECT INGUINAL-HERNIA AMONG BEDOUINS
Authors: GROVER VK NUR AMA USHA R FARAG TI SABRY MA
Citation: Vk. Grover et al., INDIRECT INGUINAL-HERNIA AMONG BEDOUINS, Journal of Medical Genetics, 33(10), 1996, pp. 887-887
DE-NOVO DIRECT DUPLICATION 7P(P11.2-]PTER) IN AN ARAB CHILD WITH MCA MR SYNDROME - TRISOMY 7P A DELINEATED SYNDROME/
Authors: REDHA MA MURTHY DSK ALAWADI SA ALSULAIMAN IS SABRY MA ELBAHEY SA FARAG TI
Citation: Ma. Redha et al., DE-NOVO DIRECT DUPLICATION 7P(P11.2-]PTER) IN AN ARAB CHILD WITH MCA MR SYNDROME - TRISOMY 7P A DELINEATED SYNDROME/, Annales de genetique, 39(1), 1996, pp. 5-9
RECURRENT REGULAR TRISOMY-21 IN 2 BEDOUIN FAMILIES - PARENTAL MOSAICISM VERSUS GENETIC PREDISPOSITION (VOL 38, PG 217, 1995)
Authors: KRISHNAMURTHY DS FARAG TI
Citation: Ds. Krishnamurthy et Ti. Farag, RECURRENT REGULAR TRISOMY-21 IN 2 BEDOUIN FAMILIES - PARENTAL MOSAICISM VERSUS GENETIC PREDISPOSITION (VOL 38, PG 217, 1995), Annales de genetique, 39(1), 1996, pp. 50-50
FAMILIAL RICHNER-HANHART-SYNDROME IN KUWAIT - 12-YEAR CLINICAL REASSESSMENT BY A MULTIDISCIPLINARY APPROACH
Authors: ELBADRAMANY MH FAWZY AR FARAG TI
Citation: Mh. Elbadramany et al., FAMILIAL RICHNER-HANHART-SYNDROME IN KUWAIT - 12-YEAR CLINICAL REASSESSMENT BY A MULTIDISCIPLINARY APPROACH, American journal of medical genetics, 60(5), 1995, pp. 353-355
RIGHT UPPER-LIMB BUD TRIPLICATION AND POLYTHELIA, LEFT-SIDED HEMIHYPERTROPHY AND CONGENITAL HIP DISLOCATION, FACIAL DYSMORPHISM, CONGENITALHEART-DISEASE, AND SCOLIOSIS - DISORGANIZATION-LIKE SPECTRUM OR PATTERNING GENE DEFECT
Authors: SABRY MA ALSALEH Q ALSAWAN R ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., RIGHT UPPER-LIMB BUD TRIPLICATION AND POLYTHELIA, LEFT-SIDED HEMIHYPERTROPHY AND CONGENITAL HIP DISLOCATION, FACIAL DYSMORPHISM, CONGENITALHEART-DISEASE, AND SCOLIOSIS - DISORGANIZATION-LIKE SPECTRUM OR PATTERNING GENE DEFECT, Journal of Medical Genetics, 32(7), 1995, pp. 555-556
SWYER SYNDROME - AN UNUSUAL PRESENTATION
Authors: MORSY AH ALFADLY A MOKHTAR S ELAASAR EM FARAG TI
Citation: Ah. Morsy et al., SWYER SYNDROME - AN UNUSUAL PRESENTATION, International journal of gynaecology and obstetrics, 49(2), 1995, pp. 185-186
RECURRENT REGULAR TRISOMY-21 IN 2 BEDOUIN FAMILIES - PARENTAL MOSAICISM VERSUS GENETIC PREDISPOSITION
Authors: MURTHY DSK FARAG TI
Citation: Dsk. Murthy et Ti. Farag, RECURRENT REGULAR TRISOMY-21 IN 2 BEDOUIN FAMILIES - PARENTAL MOSAICISM VERSUS GENETIC PREDISPOSITION, Annales de genetique, 38(4), 1995, pp. 217-224
AUTOSOMAL RECESSIVE COMMON VARIABLE IMMUNODEFICIENCY REPORTS OF 7 RELATED-CHILDREN IN A BEDOUIN KINDRED
Authors: KANDIL HH GHULAM AS THALLAB FS ALGHANIM MM FARAG TI
Citation: Hh. Kandil et al., AUTOSOMAL RECESSIVE COMMON VARIABLE IMMUNODEFICIENCY REPORTS OF 7 RELATED-CHILDREN IN A BEDOUIN KINDRED, American journal of human genetics, 57(4), 1995, pp. 511-511
JOUBERT-SYNDROME AMONG BEDOUINS - AN UNDER ESTIMATE
Authors: RAJARAM U UMA R TAHSEEN K ARAFAT R ALGHANIM MM FARAG TI
Citation: U. Rajaram et al., JOUBERT-SYNDROME AMONG BEDOUINS - AN UNDER ESTIMATE, American journal of human genetics, 57(4), 1995, pp. 580-580
PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS
Authors: ALGHANIM MM KANDIL HH ABUTALEB MA FARAG TI
Citation: Mm. Alghanim et al., PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS, American journal of human genetics, 57(4), 1995, pp. 1768-1768
A POSSIBLE NEW VARIANT OF NONSYNDROMIC LISSENCEPHALY, ASSOCIATED WITHMYOCLONIC EPILEPSY
Authors: FARAH S RUDWAN M KHAFAGI S KHURAIBET A QASRAWI B ALBUSAIRI W HASSAN M HASSEEB N ELGAMAL SA SABRY MA FARAG TI
Citation: S. Farah et al., A POSSIBLE NEW VARIANT OF NONSYNDROMIC LISSENCEPHALY, ASSOCIATED WITHMYOCLONIC EPILEPSY, American journal of human genetics, 57(4), 1995, pp. 1773-1773
A POSSIBLE NEW CRANIO FACIO FRONTO DIGITAL DYSPLASIA
Authors: QASRAWI BM ELGAMAL SA FARAG TI ALAWADI SA ALGENDI II SABRY MA
Citation: Bm. Qasrawi et al., A POSSIBLE NEW CRANIO FACIO FRONTO DIGITAL DYSPLASIA, American journal of human genetics, 57(4), 1995, pp. 1778-1778
A POSSIBLE NEW SYNDROMIC SITUS-INVERSUS TOTALIS IN AN INSTITUTIONALIZED PATIENT
Authors: SABRY MA MUBASHIR MA HASSEEB N ALAWADI SA FARAH SA QASRAWI B ALDABBOUS RM ALBUSAIRI W FARAG TI
Citation: Ma. Sabry et al., A POSSIBLE NEW SYNDROMIC SITUS-INVERSUS TOTALIS IN AN INSTITUTIONALIZED PATIENT, American journal of human genetics, 57(4), 1995, pp. 1782-1782
Risultati: 1-25 | 26-37