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Results: 1-25 | 26-28
Results: 1-25/28
AUTOSOMAL RECESSIVE SYNDROME OF MACROCEPHALY, MULTIPLE EPIPHYSEAL DYSPLASIA AND DISTINCTIVE FACIAL APPEARANCE
Authors: ALGAZALI LI BAKALINOVA D
Citation: Li. Algazali et D. Bakalinova, AUTOSOMAL RECESSIVE SYNDROME OF MACROCEPHALY, MULTIPLE EPIPHYSEAL DYSPLASIA AND DISTINCTIVE FACIAL APPEARANCE, Clinical dysmorphology, 7(3), 1998, pp. 177-184
MENTAL-RETARDATION, IRIS COLOBOMA, OPTIC ATROPHY AND DISTINCTIVE FACIAL APPEARANCE IN 2 SIBS
Authors: ALGAZALI LI
Citation: Li. Algazali, MENTAL-RETARDATION, IRIS COLOBOMA, OPTIC ATROPHY AND DISTINCTIVE FACIAL APPEARANCE IN 2 SIBS, Clinical dysmorphology, 7(3), 1998, pp. 201-203
CENTRAL-NERVOUS-SYSTEM MALFORMATIONS, DENSE BONES AND FACIAL DYSMORPHISM - A NEW AUTOSOMAL RECESSIVE SYNDROME
Authors: ALGAZALI LI BAKALINOVA D BAKIR M
Citation: Li. Algazali et al., CENTRAL-NERVOUS-SYSTEM MALFORMATIONS, DENSE BONES AND FACIAL DYSMORPHISM - A NEW AUTOSOMAL RECESSIVE SYNDROME, Clinical dysmorphology, 7(2), 1998, pp. 123-126
XK APROSENCEPHALY
Authors: ALGAZALI LI BAKALINOVA D BAKIR M NATH KNR
Citation: Li. Algazali et al., XK APROSENCEPHALY, Clinical dysmorphology, 7(2), 1998, pp. 143-147
LEARNING-DISORDERS IN SCHOOL-GOING CHILDREN - DETECTION AND DIAGNOSIS
Authors: EAPEN V ALGAZALI LI BINOTHMAN S PRAMATHAN T
Citation: V. Eapen et al., LEARNING-DISORDERS IN SCHOOL-GOING CHILDREN - DETECTION AND DIAGNOSIS, Journal of tropical pediatrics, 44(4), 1998, pp. 192-193
A GENETIC ETIOLOGIC SURVEY OF SEVERE CHILDHOOD DEAFNESS IN THE UNITED-ARAB-EMIRATES
Authors: ALGAZALI LI
Citation: Li. Algazali, A GENETIC ETIOLOGIC SURVEY OF SEVERE CHILDHOOD DEAFNESS IN THE UNITED-ARAB-EMIRATES, Journal of tropical pediatrics, 44(3), 1998, pp. 157-160
ORGANIZATION OF THE HUMAN PAX4 GENE AND ITS EXCLUSION AS A CANDIDATE FOR THE WOLCOTT-RALLISON-SYNDROME
Authors: BONTHRON DT DUNLOP N BARR DGD ELSANOUSI AA ALGAZALI LI
Citation: Dt. Bonthron et al., ORGANIZATION OF THE HUMAN PAX4 GENE AND ITS EXCLUSION AS A CANDIDATE FOR THE WOLCOTT-RALLISON-SYNDROME, Journal of Medical Genetics, 35(4), 1998, pp. 288-292
THE SYNDROME OF HYPOPARATHYROIDISM, SEVERE GROWTH FAILURE, DEVELOPMENTAL DELAY AND DISTINCTIVE FACIES
Authors: ALGAZALI LI DAWODU A
Citation: Li. Algazali et A. Dawodu, THE SYNDROME OF HYPOPARATHYROIDISM, SEVERE GROWTH FAILURE, DEVELOPMENTAL DELAY AND DISTINCTIVE FACIES, Clinical dysmorphology, 6(3), 1997, pp. 233-237
FIBROCHONDROGENESIS - CLINICAL AND RADIOLOGICAL FEATURES
Authors: ALGAZALI LI BAKALINOVA D BAKIR M DAWODU A
Citation: Li. Algazali et al., FIBROCHONDROGENESIS - CLINICAL AND RADIOLOGICAL FEATURES, Clinical dysmorphology, 6(2), 1997, pp. 157-163
ABNORMAL MYELINATION IN PEROXISOMAL ISOLATED DIHYDROXYACETONE-PHOSPHATE ACYLTRANSFERASE DEFICIENCY
Authors: SZTRIHA LA NORK MP ABDULRAZZAQ YM ALGAZALI LI BAKALINOVA DB
Citation: La. Sztriha et al., ABNORMAL MYELINATION IN PEROXISOMAL ISOLATED DIHYDROXYACETONE-PHOSPHATE ACYLTRANSFERASE DEFICIENCY, Pediatric neurology, 16(3), 1997, pp. 232-236
UNITED-ARAB-EMIRATES POPULATION-DATA ON 3 DNA TETRAMERIC SHORT TANDEMREPEAT LOCI - HUMTHO1, TPOX AND CSF1PO - DERIVED USING MULTIPLEX POLYMERASE CHAIN-REACTION AND MANUAL TYPING
Authors: BAYOUMI RA ALGAZALI LI JAFFER U NUREKAMAL MSA DAWODU A BENER A EAPEN V BUDOWLE B
Citation: Ra. Bayoumi et al., UNITED-ARAB-EMIRATES POPULATION-DATA ON 3 DNA TETRAMERIC SHORT TANDEMREPEAT LOCI - HUMTHO1, TPOX AND CSF1PO - DERIVED USING MULTIPLEX POLYMERASE CHAIN-REACTION AND MANUAL TYPING, Electrophoresis, 18(9), 1997, pp. 1637-1640
GENETIC-HETEROGENEITY IN SCHWARTZ-JAMPEL-SYNDROME - 2 FAMILIES WITH NEONATAL SCHWARTZ-JAMPEL-SYNDROME DO NOT MAP TO HUMAN-CHROMOSOME-1P34-P36.1
Authors: BROWN KA ALGAZALI LI MOYNIHAN LM LENCH NJ MARKHAM AF MUELLER RF
Citation: Ka. Brown et al., GENETIC-HETEROGENEITY IN SCHWARTZ-JAMPEL-SYNDROME - 2 FAMILIES WITH NEONATAL SCHWARTZ-JAMPEL-SYNDROME DO NOT MAP TO HUMAN-CHROMOSOME-1P34-P36.1, Journal of Medical Genetics, 34(8), 1997, pp. 685-687
FURTHER DELINEATION OF NEVO SYNDROME
Authors: ALGAZALI LI BAKALINOVA D VARADY E SCORER J NORK M
Citation: Li. Algazali et al., FURTHER DELINEATION OF NEVO SYNDROME, Journal of Medical Genetics, 34(5), 1997, pp. 366-370
CONSANGUINEOUS MARRIAGES IN THE UNITED-ARAB-EMIRATES
Authors: ALGAZALI LI BENER A ABDULRAZZAQ YM MICALLEF R ALKHAYAT AI GABER T
Citation: Li. Algazali et al., CONSANGUINEOUS MARRIAGES IN THE UNITED-ARAB-EMIRATES, Journal of Biosocial Science, 29(4), 1997, pp. 491-497
A STUDY OF POSSIBLE DELETERIOUS EFFECTS OF CONSANGUINITY
Authors: ABDULRAZZAQ YM BENER A ALGAZALI LI ALKHAYAT AI MICALLEF R GABER T
Citation: Ym. Abdulrazzaq et al., A STUDY OF POSSIBLE DELETERIOUS EFFECTS OF CONSANGUINITY, Clinical genetics, 51(3), 1997, pp. 167-173
AUTOSOMAL RECESSIVE NON-SYNDROMIC DEAFNESS (DFNA3 DFNB1) - CONNEXIN-26 MUTATION ANALYSIS IN PAKISTANI, MIDDLE-EASTERN AND CAUCASIAN POPULATIONS/
Authors: LENCH NJ MUELLER RF HOUSEMAN M MIDDLETON A KARBANI G JANJUA AH NEWTON V PARRY G ALGAZALI LI MARKHAM AF
Citation: Nj. Lench et al., AUTOSOMAL RECESSIVE NON-SYNDROMIC DEAFNESS (DFNA3 DFNB1) - CONNEXIN-26 MUTATION ANALYSIS IN PAKISTANI, MIDDLE-EASTERN AND CAUCASIAN POPULATIONS/, American journal of human genetics, 61(4), 1997, pp. 107-107
A SYNDROME OF SHORT STATURE, MENTAL-RETARDATION, FACIAL DYSMORPHISM, SHORT WEBBED NECK, SKIN CHANGES AND CONGENITAL HEART-DISEASE
Authors: ALGAZALI LI AZIZ SAA SALEM F
Citation: Li. Algazali et al., A SYNDROME OF SHORT STATURE, MENTAL-RETARDATION, FACIAL DYSMORPHISM, SHORT WEBBED NECK, SKIN CHANGES AND CONGENITAL HEART-DISEASE, Clinical dysmorphology, 5(4), 1996, pp. 321-327
SPONDYLO-META-EPIPHYSEAL DYSPLASIA, SHORT LIMB, ABNORMAL CALCIFICATION TYPE
Authors: ALGAZALI LI BAKALINOVA D SZTRIHA L
Citation: Li. Algazali et al., SPONDYLO-META-EPIPHYSEAL DYSPLASIA, SHORT LIMB, ABNORMAL CALCIFICATION TYPE, Clinical dysmorphology, 5(3), 1996, pp. 197-206
SETLEIS SYNDROME - AUTOSOMAL RECESSIVE OR AUTOSOMAL-DOMINANT INHERITANCE
Authors: ALGAZALI LI ALTALABANI J
Citation: Li. Algazali et J. Altalabani, SETLEIS SYNDROME - AUTOSOMAL RECESSIVE OR AUTOSOMAL-DOMINANT INHERITANCE, Clinical dysmorphology, 5(3), 1996, pp. 249-253
A NEW LETHAL NEONATAL SHORT LIMB DWARFISM
Authors: ALGAZALI LI DEVADAS K HALL CM
Citation: Li. Algazali et al., A NEW LETHAL NEONATAL SHORT LIMB DWARFISM, Clinical dysmorphology, 5(2), 1996, pp. 159-164
NEONATAL SCHWARTZ-JAMPEL SYNDROME - A COMMON AUTOSOMAL RECESSIVE SYNDROME IN THE UNITED-ARAB-EMIRATES
Authors: ALGAZALI LI VARGHESE M VARADY E ALTALABANI J SCORER J BALTALINOVA D
Citation: Li. Algazali et al., NEONATAL SCHWARTZ-JAMPEL SYNDROME - A COMMON AUTOSOMAL RECESSIVE SYNDROME IN THE UNITED-ARAB-EMIRATES, Journal of Medical Genetics, 33(3), 1996, pp. 203-211
CONSANGUINITY AND ASSOCIATED SOCIODEMOGRAPHIC FACTORS IN THE UNITED-ARAB-EMIRATES
Authors: BENER A ABDULRAZZAQ YM ALGAZALI LI MICALLEF R ALKHAYAT AI GABER T
Citation: A. Bener et al., CONSANGUINITY AND ASSOCIATED SOCIODEMOGRAPHIC FACTORS IN THE UNITED-ARAB-EMIRATES, Human heredity, 46(5), 1996, pp. 256-264
THE PROFILE OF MAJOR CONGENITAL-ABNORMALITIES IN THE UNITED-ARAB-EMIRATES (UAE) POPULATION
Authors: ALGAZALI LI DAWODU AH SABARINATHAN K VARGHESE M
Citation: Li. Algazali et al., THE PROFILE OF MAJOR CONGENITAL-ABNORMALITIES IN THE UNITED-ARAB-EMIRATES (UAE) POPULATION, Journal of Medical Genetics, 32(1), 1995, pp. 7-13
HOMOZYGOSITY FOR A NEW MUTATION (ILE(119)-]MET) IN THE INSULIN-RECEPTOR GENE IN 5 SIBS WITH FAMILIAL INSULIN-RESISTANCE
Authors: HONE J ACCILI D ALGAZALI LI LESTRINGANT G ORBAN T TAYLOR SI
Citation: J. Hone et al., HOMOZYGOSITY FOR A NEW MUTATION (ILE(119)-]MET) IN THE INSULIN-RECEPTOR GENE IN 5 SIBS WITH FAMILIAL INSULIN-RESISTANCE, Journal of Medical Genetics, 31(9), 1994, pp. 715-716
A SYNDROME OF INSULIN-RESISTANCE RESEMBLING LEPRECHAUNISM IN 5 SIBS OF CONSANGUINEOUS PARENTS (VOL 30, PG 470, 1993)
Authors: ALGAZALI LI KHALIL M DEVADAS K
Citation: Li. Algazali et al., A SYNDROME OF INSULIN-RESISTANCE RESEMBLING LEPRECHAUNISM IN 5 SIBS OF CONSANGUINEOUS PARENTS (VOL 30, PG 470, 1993), Journal of Medical Genetics, 31(1), 1994, pp. 88-88
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