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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
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
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
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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
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
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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
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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
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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
Citation: Ear. Ismail et al., NEPHROCALCINOSIS AND UROLITHIASIS IN CARBONIC-ANHYDRASE-II DEFICIENCYSYNDROME, European journal of pediatrics, 156(12), 1997, pp. 957-962
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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
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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
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
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
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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
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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
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
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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