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Results of search for 'au:"Mégarbane, A"', page 1 of 6
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Authors
Adib, S M
Ashoush, R
Bleik, J
Bouvagnet, P
Chouery, E
Claustres, M
Corbani, S
Cormier-Daire, V
Delague, V
Faivre, L
Francannet, C
Ghanem, I
Goldenberg, A
Le Merrer, M
Lefranc, G
Loiselet, J
Megarbane, A
Mégarbané, A
Salem, N
Souraty, N
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Consanguinity
Female
Genes, Recessive
Humans
Infant
Infant, Newborn
Intellectual Disability
Lebanon
Male
Mutation
Pedigree
Syndrome
abnormalities
diagnosis
genetics
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English
French
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Your search returned 111 results.
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1.
[The harlequin baby. Apropos of a case].
[electronic resource]
by
Megarbane, A
Producer:
19990415
In:
Le Journal medical libanais. The Lebanese medical journal
vol. 46
Availability:
No items available.
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2.
A new familial syndrome with facial abnormalities, abnormal EEG, and mental retardation.
[electronic resource]
by
Mégarbané, A
Producer:
20010823
In:
Clinical dysmorphology
vol. 10
Online resources:
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3.
Severe mental retardation with marfanoid habitus in a young Lebanese male. A diagnostic challenge.
[electronic resource]
by
Mégarbané, A
Chammas, C
Producer:
19980108
In:
Genetic counseling (Geneva, Switzerland)
vol. 8
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4.
Craniosynostosis and marfanoid habitus without mental retardation: report of a third case.
[electronic resource]
by
Mégarbané, A
Hokayem, N
Producer:
19980624
In:
American journal of medical genetics
vol. 77
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5.
Early lethal autosomal recessive enterocolitis: report of a second family.
[electronic resource]
by
Mégarbané, A
Sayad, R
Producer:
20070309
In:
Clinical genetics
vol. 71
Online resources:
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6.
Clinical manifestation of a severe neonatal progeroid syndrome.
[electronic resource]
by
Mégarbané, A
Loiselet, J
Producer:
19970612
In:
Clinical genetics
vol. 51
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7.
Does the cranio-cerebello-cardiac syndrome (3C syndrome) include abdominal malformations?
[electronic resource]
by
Mégarbané, A
Haddad, J
Producer:
19991116
In:
Clinical dysmorphology
vol. 8
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8.
Severe autosomal dominant upper-limb mesomelic dysplasia: report of a second family.
[electronic resource]
by
Mégarbané, A
Ghanem, I
Producer:
20060615
In:
Clinical genetics
vol. 68
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9.
A cytogenetic register of down syndrome in Lebanon.
[electronic resource]
by
Zahed, L
Megarbane, A
Producer:
20050125
In:
Community genetics
vol. 1
Online resources:
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10.
Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
[electronic resource]
by
Mégarbané, A
Abi Moussa, M
Producer:
19970819
In:
Genetic counseling (Geneva, Switzerland)
vol. 8
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11.
Congenital malformations and genetic diseases in comic books.
[electronic resource]
by
Mégarbané, A
Adib, S M
Producer:
20030827
In:
Genetic counseling (Geneva, Switzerland)
vol. 14
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12.
[Pre-symptomatic diagnosis of severe hereditary diseases with late onset in Lebanon: a choice or a necessity?].
[electronic resource]
by
Medlej-Hashim, M
Mégarbané, A
Producer:
20060307
In:
Sante publique (Vandoeuvre-les-Nancy, France)
vol. 17
Online resources:
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13.
Severe mental retardation, short stature, facial anomalies, joint laxity, and dislocations in two sisters: previously undescribed MCA/MR syndrome.
[electronic resource]
by
Mégarbané, A
Cormier-Daire, V
Producer:
20010816
In:
American journal of medical genetics
vol. 102
Online resources:
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14.
Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family.
[electronic resource]
by
Mégarbané, A
Tomey, K
Wakim, G
Producer:
19980123
In:
American journal of medical genetics
vol. 73
Online resources:
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15.
Ophthalmo-acromelic syndrome (Waardenburg) with split hand and polydactyly.
[electronic resource]
by
Mégarbané, A
Souraty, N
Tamraz, J
Producer:
19981202
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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16.
Four sibs with dislocated elbows, bowed tibiae, scoliosis, deafness, cataract, microcephaly, and mental retardation: a new MCA/MR syndrome.
[electronic resource]
by
Mégarbané, A
Kharrat, K
Kreichati, G
Producer:
19981110
In:
Journal of medical genetics
vol. 35
Online resources:
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17.
Tetraamelia associated with a syrinx: fortuitous association or clue?
[electronic resource]
by
Megarbane, A
Tamraz, J
Haddad, S
Producer:
19970326
In:
Clinical dysmorphology
vol. 6
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18.
[Cockayne syndrome in Lebanon. Description of 3 cases and review of the literature].
[electronic resource]
by
Jabre, P
Mezzina, M
Megarbane, A
Producer:
19991007
In:
Le Journal medical libanais. The Lebanese medical journal
vol. 47
Availability:
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19.
[Mechanical raising of the chondrodiaphragmatic roof in surgery of the upper level of the abdomen].
[electronic resource]
by
FRUCHAUD, H
LESSERTISSEUR, J
MEGARBANE, A
Producer:
20000701
In:
Memoires. Academie de chirurgie (France)
vol. 84
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20.
Prenatal ultrasonography: clinical and radiological findings in a boy with fibrochondrogenesis.
[electronic resource]
by
Mégarbané, A
Haddad, S
Berjaoui, L
Producer:
19981217
In:
American journal of perinatology
vol. 15
Online resources:
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