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1-19
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Results: 19
Authors:
MEGARBANE A
HAWAT N
CHEDID P
BLEIK J
DELEZOIDE A
Citation: A. Megarbane et al., BRANCHIOOCULOFACIAL SYNDROME-ASSOCIATED WITH A WHITE FORELOCK, Clinical dysmorphology, 7(3), 1998, pp. 221-223
Authors:
MEGARBANE A
HADDAD S
BERJAOUI L
Citation: A. Megarbane et al., PRENATAL ULTRASONOGRAPHY - CLINICAL AND RADIOLOGICAL FINDINGS IN A BOY WITH FIBROCHONDROGENESIS, American journal of perinatology, 15(7), 1998, pp. 403-407
Authors:
SAOUDA M
MANSOUR A
MOGLABEY YB
ELZIR E
MUSTAPHA M
CHAIB H
NEHME A
MEGARBANE A
LOISELET J
PETIT C
SLIM R
Citation: M. Saouda et al., THE USHER-SYNDROME IN THE LEBANESE POPULATION AND FURTHER REFINEMENT OF THE USH2A CANDIDATE REGION, Human genetics, 103(2), 1998, pp. 193-198
Authors:
MEGARBANE A
HOKAYEM N
Citation: A. Megarbane et N. Hokayem, CRANIOSYNOSTOSIS AND MARFANOID HABITUS WITHOUT MENTAL-RETARDATION - REPORT OF A 3RD CASE, American journal of medical genetics, 77(2), 1998, pp. 170-171
Authors:
MEGARBANE A
NOUJEIM Z
FABRE M
KALOUSTIAN VMD
Citation: A. Megarbane et al., NEW FORM OF HIDROTIC ECTODERMAL DYSPLASIA IN A LEBANESE FAMILY, American journal of medical genetics, 75(2), 1998, pp. 196-199
Authors:
MEGARBANE A
KHARRAT K
KREICHATI G
Citation: A. Megarbane et al., 4 SIBS WITH DISLOCATED ELBOWS, BOWED TIBIAE, SCOLIOSIS, DEAFNESS, CATARACT, MICROCEPHALY, AND MENTAL-RETARDATION - A NEW MCA MR SYNDROME/, Journal of Medical Genetics, 35(9), 1998, pp. 755-758
Authors:
MEGARBANE A
LEMERRER M
ELKALLAB K
Citation: A. Megarbane et al., PTOSIS, DOWN-SLANTING PALPEBRAL FISSURES, HYPERTELORISM, SEIZURES ANDMENTAL-RETARDATION - A POSSIBLE NEW MCA MR SYNDROME/, Clinical dysmorphology, 6(3), 1997, pp. 239-244
Authors:
MEGARBANE A
TAMRAZ J
HADDAD S
Citation: A. Megarbane et al., TETRAAMELIA ASSOCIATED WITH A SYRINX - FORTUITOUS ASSOCIATION OR CLUE, Clinical dysmorphology, 6(1), 1997, pp. 81-84
Authors:
ORTI R
MEGARBANE A
MAUNOURY C
VANBROECKHOVEN C
SINET PM
DELABAR JM
Citation: R. Orti et al., HIGH-RESOLUTION PHYSICAL MAPPING OF A 6.7-MB YAC CONTIG SPANNING A REGION CRITICAL FOR THE MONOSOMY-21 PHENOTYPE IN 21Q21.3-Q22.1, Genomics, 43(1), 1997, pp. 25-33
Authors:
DESGEORGES M
MEGARBANE A
GUITTARD C
CARLES S
LOISELET J
DEMAILLE J
CLAUSTRES M
Citation: M. Desgeorges et al., CYSTIC-FIBROSIS IN LEBANON - DISTRIBUTION OF CFTR MUTATIONS AMONG ARAB COMMUNITIES, Human genetics, 100(2), 1997, pp. 279-283
Authors:
ORTI R
MEGARBANE A
CHETTOUH Z
MAUNOURY C
DUFRESNEZACCHARIA MC
VANBROECKHOVEN C
SINET PM
DELABAR JM
Citation: R. Orti et al., A 5.9-MB YAC CONTIG SPANNING THE APP-SOD1 REGION CRITICAL FOR THE MONOSOMY-21 SYNDROME, Cytogenetics and cell genetics, 79(1-2), 1997, pp. 35-35
Authors:
MEGARBANE A
TOMEY K
WAKIM G
Citation: A. Megarbane et al., CONGENITAL GLAUCOMA, LIMB DEFORMITIES, SKELETAL DYSPLASIA, AND FACIALANOMALIES - REPORT OF ANOTHER FAMILY, American journal of medical genetics, 73(1), 1997, pp. 67-71
Authors:
MEGARBANE A
SOURATY N
PRIEUR M
THEOPHILE D
CHEDID P
AUGE J
VEKEMANS M
Citation: A. Megarbane et al., INTERSTITIAL DUPLICATION OF THE SHORT ARM OF CHROMOSOME-2 - REPORT OFA NEW CASE AND REVIEW, Journal of Medical Genetics, 34(9), 1997, pp. 783-786
Authors:
MEGARBANE A
LOISELET J
Citation: A. Megarbane et J. Loiselet, CLINICAL MANIFESTATION OF A SEVERE NEONATAL PROGEROID SYNDROME, Clinical genetics, 51(3), 1997, pp. 200-204
Authors:
MEGARBANE A
SOURATY N
THEOPHILE D
VEKEMANS M
SAMARAS L
GHORAYEB Z
Citation: A. Megarbane et al., TRISOMY FOR THE DISTAL SEGMENT OF THE SHORT ARM OF CHROMOSOME-17 IN ABOY WITH MILD MENTAL-RETARDATION AND SOME DYSMORPHIC FEATURES, Annales de genetique, 40(1), 1997, pp. 55-59
Authors:
PARIS D
TOYAMA K
MEGARBANE A
CASANOVA M
SINET PM
LONDON J
Citation: D. Paris et al., RAPID FLUORESCENCE IN-SITU HYBRIDIZATION ON INTERPHASIC NUCLEI TO DISCRIMINATE BETWEEN HOMOZYGOUS AND HETEROZYGOUS TRANSGENIC MICE, Transgenic research, 5(6), 1996, pp. 397-403
Authors:
ORTI R
MEGARBANE A
CHETTOUH Z
DUFRESNEZACHARIA MC
DAHMANE N
VANBROECKHOVEN C
SINET PM
DELABAR JM
Citation: R. Orti et al., DEFINITION OF A REGION CRITICAL FOR THE MONOSOMY-21 SYNDROME - SOD1-APP - GENOMIC AND YAC MAPPING, Cytogenetics and cell genetics, 70(3-4), 1995, pp. 169-169
Authors:
MEGARBANE A
JOBERT AS
RETHORE MO
LEJEUNE J
PEETERS M
Citation: A. Megarbane et al., ANNOUNCEMENT OF DIAGNOSIS OF 21-TRISOMY A ND ABANDONMENT, Archives de pediatrie, 1(9), 1994, pp. 856-857
Authors:
PEETERS MA
MEGARBANE A
CATTANEO F
RETHORE MO
LEJEUNE J
Citation: Ma. Peeters et al., DIFFERENCES IN PURINE METABOLISM IN PATIENTS WITH DOWNS-SYNDROME, JIDR. Journal of intellectual disability research, 37, 1993, pp. 491-505
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