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Results of search for 'au:"Mégarbane, A"', page 2 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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21.
[Speech pathology intervention for autistic children in Lebanon: status, needs and perspectives].
[electronic resource]
by
Kouba-Hreich, E
Henri, G
Mégarbané, A
Producer:
20021010
In:
Le Journal medical libanais. The Lebanese medical journal
vol. 49
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22.
Unknown syndrome in two male sibs with hypotonia, ptosis, hand malformations, 2/3 toes syndactyly, and mental retardation.
[electronic resource]
by
Mégarbané, A
Farah, C B
Nabbout, R
Producer:
19991227
In:
Genetic counseling (Geneva, Switzerland)
vol. 10
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23.
How many phenotypes in the DTDST family chondrodysplasias?
[electronic resource]
by
Mégarbané, A
Farkh, I
Haddad-Zebauni, S
Producer:
20030213
In:
Clinical genetics
vol. 62
Online resources:
Available from publisher's website
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24.
Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type: report of a new patient and review of the literature.
[electronic resource]
by
Mégarbané, A
Ghanem, I
Le Merrer, M
Producer:
20040422
In:
American journal of medical genetics. Part A
vol. 122A
Online resources:
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25.
[Retrospective study of nine Lebanese families with fragile X syndrome and review of the literature].
[electronic resource]
by
Zafatayeff, S
Zahed, L
Souraty, N
Megarbane, A
Producer:
19990617
In:
Le Journal medical libanais. The Lebanese medical journal
vol. 46
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26.
[Megalencephalic leucoencephalopathy with subcortical cysts: a study of a Lebanese family and a review of the literature].
[electronic resource]
by
Koussa, S
Roukoz, H
Rizk, T
Mégarbané, A
Producer:
20050503
In:
Revue neurologique
vol. 161
Online resources:
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27.
[Direct surgery of the lower portion of the common bile duct].
[electronic resource]
by
FRUCHAUD, H
ARIS, C
HALLAC, I
MEGARBANE, A
Producer:
20030501
In:
Archives des maladies de l'appareil digestif et des maladies de la nutrition
vol. 44
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28.
Ptosis, down-slanting palpebral fissures, hypertelorism, seizures and mental retardation: a possible new MCA/MR syndrome.
[electronic resource]
by
Mégarbané, A
Le Merrer, M
el Kallab, K
Producer:
19970922
In:
Clinical dysmorphology
vol. 6
Online resources:
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29.
Dysmorphology in literature: describing is not condoning.
[electronic resource]
by
Adib, S M
Mégarbané, A
Fryns, J P
Producer:
20030827
In:
Genetic counseling (Geneva, Switzerland)
vol. 14
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30.
Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family.
[electronic resource]
by
Mégarbané, A
Delague, V
Salem, N
Loiselet, J
Producer:
19991201
In:
American journal of medical genetics
vol. 87
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31.
Non-collagenic etiologies of muscle weakness with joint deformities: about two paradigmatic case reports.
[electronic resource]
by
Urtizberea, J A
Thambyayah, M
Nishino, I
Megarbane, A
Producer:
20060421
In:
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
vol. 24
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32.
International cooperation in the expansion of a newborn screening programme in Lebanon: a possible model for other programmes.
[electronic resource]
by
Khneisser, I
Adib, S M
Megarbane, A
Lukacs, Z
Producer:
20120111
In:
Journal of inherited metabolic disease
vol. 31 Suppl 2
Online resources:
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33.
Five mandibular incisors: an autosomal recessive trait?
[electronic resource]
by
Cassia, A
El-Toum, S
Feki, A
Megarbane, A
Producer:
20041109
In:
British dental journal
vol. 197
Online resources:
Available from publisher's website
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34.
[Congenital exfoliative erythroderma].
[electronic resource]
by
Mégarbané, H
Tomb, R
Klein-Tomb, L
Mégarbané, A
Producer:
20040601
In:
Annales de dermatologie et de venereologie
vol. 131
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35.
Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
[electronic resource]
by
Mégarbané, A
Choueiri, R
Bleik, J
Mezzina, M
Caillaud, C
Producer:
19990927
In:
Journal of medical genetics
vol. 36
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36.
Cost-benefit analysis: newborn screening for inborn errors of metabolism in Lebanon.
[electronic resource]
by
Khneisser, I
Adib, S
Assaad, S
Megarbane, A
Karam, P
Producer:
20160622
In:
Journal of medical screening
vol. 22
Online resources:
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37.
Microalbuminuria versus brain natriuretic peptide in cardiac hypertrophy of hypertensive rats.
[electronic resource]
by
Saliba, Y
Chouery, E
Mégarbané, A
Jabbour, H
Farès, N
Producer:
20110802
In:
Physiological research
vol. 59
Online resources:
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38.
New form of hidrotic ectodermal dysplasia in a Lebanese family.
[electronic resource]
by
Mégarbané, A
Noujeim, Z
Fabre, M
Der Kaloustian, V M
Producer:
19980324
In:
American journal of medical genetics
vol. 75
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39.
Congenital contractures, short stature, abnormal face, microcephaly, scoliosis, hip dislocation, and severe psychomotor retardation in two unrelated girls. a new MCA/MR syndrome?
[electronic resource]
by
Mégarbané, A
Ghanem, I
Romana, S
Gosset, P
Caillaud, C
Producer:
20030103
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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40.
[Frontal pseudo-tumoral form of adrenoleukodystrophy].
[electronic resource]
by
Koussa, S
Megarbane, A
Rizk, T
Tamraz, J
Chemaly, R
Producer:
20010202
In:
Revue neurologique
vol. 156
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