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Results: 1-25 | 26-33
Results: 1-25/33
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
CUTIS-VERTICIS-GYRATA-MENTAL-DEFICIENCY-SYNDROME - REPORT OF A CASE WITH UNUSUAL NEURORADIOLOGICAL FINDINGS
Authors: FARAH S FARAG T SABRY MA SIMEONOV ST ALKHATTAM S ABULHASSAN SJ QUASRAWI B ALBUSAIRI W ALAWADI SA
Citation: S. Farah et al., CUTIS-VERTICIS-GYRATA-MENTAL-DEFICIENCY-SYNDROME - REPORT OF A CASE WITH UNUSUAL NEURORADIOLOGICAL FINDINGS, Clinical dysmorphology, 7(2), 1998, pp. 131-134
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
BRIEF CLINICAL REPORT - CRANIOFACIAL DYSSYNOSTOSIS WITH CRYPTORCHIDISM AND NORMAL STATURE
Authors: ALTORKI NA SABRY MA ALTAWARI A ALKANDARI NH ALAWADI SA
Citation: Na. Altorki et al., BRIEF CLINICAL REPORT - CRANIOFACIAL DYSSYNOSTOSIS WITH CRYPTORCHIDISM AND NORMAL STATURE, American journal of medical genetics, 79(1), 1998, pp. 5-7
ROBINOW-SYNDROME - REPLY
Authors: SABRY MA ISMAIL EAR ALTORKI NA FARAH S
Citation: Ma. Sabry et al., ROBINOW-SYNDROME - REPLY, Journal of Medical Genetics, 35(4), 1998, pp. 350-350
GENOTYPIC PHENOTYPIC HETEROGENEITY OF KENNY-CAFFEY-SYNDROME/
Authors: SABRY MA ZAKI M SHALTOUT A
Citation: Ma. Sabry et al., GENOTYPIC PHENOTYPIC HETEROGENEITY OF KENNY-CAFFEY-SYNDROME/, Journal of Medical Genetics, 35(12), 1998, pp. 1054-1055
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
KENNY-CAFFEY-SYNDROME IS PART OF THE CATCH-22 HAPLOINSUFFICIENCY CLUSTER
Authors: SABRY MA ZAKI M HASSAN SJA RAMADAN DG RASOOL MAA ALAWADI SA ALSALEH Q
Citation: Ma. Sabry et al., KENNY-CAFFEY-SYNDROME IS PART OF THE CATCH-22 HAPLOINSUFFICIENCY CLUSTER, Journal of Medical Genetics, 35(1), 1998, pp. 31-36
VALUE OF CA-242 IN COMPLEMENTING CONVENTIONAL DIAGNOSTIC METHODS IN PANCREATIC-CARCINOMA IN EGYPTIAN PATIENTS
Authors: ELMISSIRY AG FAHMY HM SABRY MA AMER HA ELBANNA MR ALY SA
Citation: Ag. Elmissiry et al., VALUE OF CA-242 IN COMPLEMENTING CONVENTIONAL DIAGNOSTIC METHODS IN PANCREATIC-CARCINOMA IN EGYPTIAN PATIENTS, Clinical chemistry, 44, 1998, pp. 149-149
VALUE OF CA-242 IN COMPLEMENTING CONVENTIONAL DIAGNOSTIC METHODS IN PANCREATIC-CARCINOMA IN EGYPTIAN PATIENTS
Authors: FAHMY HM SABRY MA AMER HA ELBANNA MR ALY SA ELMISSIRY AG
Citation: Hm. Fahmy et al., VALUE OF CA-242 IN COMPLEMENTING CONVENTIONAL DIAGNOSTIC METHODS IN PANCREATIC-CARCINOMA IN EGYPTIAN PATIENTS, Clinical chemistry, 44, 1998, pp. 174-174
NONHEMATOLOGICAL TRAITS ASSOCIATED WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-1 - A NEW ENTITY EMERGING
Authors: SABRY MA ZAKI M ALAWADI SA ALSALEH Q MATTAR MS
Citation: Ma. Sabry et al., NONHEMATOLOGICAL TRAITS ASSOCIATED WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-1 - A NEW ENTITY EMERGING, Clinical dysmorphology, 6(3), 1997, pp. 205-212
GERODERMIA OSTEODYSPLASTICA IN A BEDOUIN SIBSHIP - FURTHER DELINEATION OF THE SYNDROME
Authors: ALTORKI NA ALAWADI SA CINDROHEBERIE L SABRY MA
Citation: Na. Altorki et al., GERODERMIA OSTEODYSPLASTICA IN A BEDOUIN SIBSHIP - FURTHER DELINEATION OF THE SYNDROME, Clinical dysmorphology, 6(1), 1997, pp. 51-55
GENOTYPIC PHENOTYPIC HETEROGENEITY OF SELECTIVE VITAMIN-B12 MALABSORPTION (GRASBECK-IMERSLUND SYNDROME) IN 2 BEDOUIN FAMILIES/
Authors: ISMAIL EAR ALSALEH Q SABRY MA ALGHANIM M ZAKI M
Citation: Ear. Ismail et al., GENOTYPIC PHENOTYPIC HETEROGENEITY OF SELECTIVE VITAMIN-B12 MALABSORPTION (GRASBECK-IMERSLUND SYNDROME) IN 2 BEDOUIN FAMILIES/, Acta paediatrica, 86(4), 1997, pp. 424-425
NEPHROCALCINOSIS AND UROLITHIASIS IN CARBONIC-ANHYDRASE-II DEFICIENCYSYNDROME
Authors: ISMAIL EAR SAAD SA SABRY MA
Citation: Ear. Ismail et al., NEPHROCALCINOSIS AND UROLITHIASIS IN CARBONIC-ANHYDRASE-II DEFICIENCYSYNDROME, European journal of pediatrics, 156(12), 1997, pp. 957-962
HEREDITARY SPASTIC PARAPARESIS WITH DISTAL MUSCLE WASTING, MICROCEPHALY, MENTAL-RETARDATION, ARACHNODACTYLY AND TREMORS - NEW ENTITY
Authors: FARAH S SABRY MA ALSHUBAILI AFK ANIM JT HUSSAIN JM MONTASER MA SHARFUDDIN KM
Citation: S. Farah et al., HEREDITARY SPASTIC PARAPARESIS WITH DISTAL MUSCLE WASTING, MICROCEPHALY, MENTAL-RETARDATION, ARACHNODACTYLY AND TREMORS - NEW ENTITY, Clinical neurology and neurosurgery, 99(1), 1997, pp. 66-70
LOWRY-MACLEAN-SYNDROME WITH OSTEOPENIC BONES AND POSSIBLE AUTOSOMAL-DOMINANT INHERITANCE IN A BEDOUIN FAMILY
Authors: ALTORKI NA SABRY MA ALAWADI SA ALTARKEIT N
Citation: Na. Altorki et al., LOWRY-MACLEAN-SYNDROME WITH OSTEOPENIC BONES AND POSSIBLE AUTOSOMAL-DOMINANT INHERITANCE IN A BEDOUIN FAMILY, American journal of medical genetics, 73(4), 1997, pp. 491-492
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
UNUSUAL TRAITS ASSOCIATED WITH ROBINOW-SYNDROME
Authors: SABRY MA ISMAIL EAR ALNAGGAR RL ALTORKI NA FARAH S ALAWADI SA OBENBERGEROVA D BASTAKI L
Citation: Ma. Sabry et al., UNUSUAL TRAITS ASSOCIATED WITH ROBINOW-SYNDROME, Journal of Medical Genetics, 34(9), 1997, pp. 736-740
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
SAGITTAL CORONAL CRANIOSYNOSTOSIS ASSOCIATED WITH BALANCED RECIPROCALTRANSLOCATION [T(2-8)(2P16-8P22)] IN AN ARAB GIRL/
Authors: ALTORKI NA ABULHASSAN SJ SABRY MA RASOOL MAA ALJAMEH I ALAWADI SA
Citation: Na. Altorki et al., SAGITTAL CORONAL CRANIOSYNOSTOSIS ASSOCIATED WITH BALANCED RECIPROCALTRANSLOCATION [T(2-8)(2P16-8P22)] IN AN ARAB GIRL/, American journal of human genetics, 61(4), 1997, pp. 2174-2174
IDENTIFICATION OF CHROMOSOME 15Q11-12 HAPLO-INSUFFIENCY IN THE AUTISTIC DISORDER
Authors: SABRY MA ALSHUBAILI A MAGHRABI MA FARAH S ABULHASSAN SJ RASOOL MAA ALAWADI SA
Citation: Ma. Sabry et al., IDENTIFICATION OF CHROMOSOME 15Q11-12 HAPLO-INSUFFIENCY IN THE AUTISTIC DISORDER, American journal of human genetics, 61(4), 1997, pp. 2193-2193
MARINESCO-SJOGREN-SYNDROME IN A BEDOUIN FAMILY
Authors: FARAH S SABRY MA KHURAIBET AJ ANIM JT QUASRAWI B ALKHATAM S ALBUSAIRI W HUSSEIN JM KHAN RA ALAWADI SA
Citation: S. Farah et al., MARINESCO-SJOGREN-SYNDROME IN A BEDOUIN FAMILY, Acta neurologica Scandinavica, 96(6), 1997, pp. 387-391
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
Risultati: 1-25 | 26-33