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Search Results - Attia‐Sobol, Jocelyne
Search Results - Attia‐Sobol, Jocelyne
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Cerebral dysgenesis does not exclude OFD I syndrome
by
Thauvin-Robinet, Christel
,
Lesca, Gaëtan
,
Aral, Bernard
,
Gigot, Nadège
,
Lambert, Sandy
,
Gueneau, Lucie
,
Macca, Marina
,
Franco, Brunella
,
Huet, Frédéric
,
Zabot, Marie-Thérèse
,
Attié-Bitach, Tania
,
Attia-Sobol, Jocelyne
,
Faivre, Laurence
Published in
American journal of medical genetics. Part A
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Campomelic acampomelic dysplasia presenting with increased nuchal translucency in the first trimester
by
Michel-Calemard, Laurence
,
Lesca, Gaëtan
,
Morel, Yves
,
Boggio, Dominique
,
Plauchu, Henri
,
Attia-Sobol, Jocelyne
Published in
Prenatal diagnosis
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Focal sonographic periventricular pattern associated with mild ventriculomegaly in foetal cytomegalic infection revealing cytomegalic encephalitis in the third trimester of pregnan...
by
Guibaud, Laurent
,
Attia-Sobol, Jocelyne
,
Buenerd, Annie
,
Foray, Patrice
,
Jacquet, Catherine
,
Champion, Fabienne
,
Arnould, Pierre
,
Pracros, Jean-Pierre
,
Golfier, François
Published in
Prenatal diagnosis
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Orofaciodigital syndrome with cerebral dysgenesis
by
Lesca, Gaetan
,
Fallet‐Bianco, Catherine
,
Plauchu, Henri
,
Vitrey, Danielle
,
Verloes, Alain
,
Attia‐Sobol, Jocelyne
Published in
American journal of medical genetics. Part A
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Hypermobility type of Ehlers-Danlos syndrome: influence of pregnancies
by
Golfier, François
,
Peyrol, Simone
,
Attia-Sobol, Jocelyne
,
Marret, Henri
,
Raudrant, Daniel
,
Plauchu, Henri
Published in
Clinical genetics
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Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations
by
AGUILELLA, Céline
,
DUBOURG, Christèle
,
ATTIA-SOBOL, Jocelyne
,
VIGNERON, Jacqueline
,
BLAYAU, Martine
,
PASQUIER, Laurent
,
LAZARO, Leila
,
ODENT, Sylvie
,
DAVID, Véronique
Published in
Human genetics
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THE SPECTRUM OF TYPE III LISSENCEPHALY: A CLINICOPATHOLOGICAL UPDATE
by
Allias, Fabienne
,
Buenerd, Annie
,
Bouvier, Raymonde
,
Attia-Sobol, Jocelyne
,
Dijoud, Frédérique
,
Clémenson, Alixe
,
Encha-Razavi, Férechté
Published in
Fetal and pediatric pathology
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Lissencephaly type III, stippled epiphyses and loose, thick skin: A new recessively inherited syndrome
by
Attia-Sobol, Jocelyne
,
Encha-Razavi, Férechté
,
Hermier, Marc
,
Vitrey, Danielle
,
Verloes, Alain
,
Plauchu, Henri
Published in
American journal of medical genetics
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Orofaciodigital syndrome with cerebral dysgenesis
by
Lesca, Gaetan
,
Fallet-Bianco, Catherine
,
Plauchu, Henri
,
Vitrey, Danielle
,
Verloes, Alain
,
Attia-Sobol, Jocelyne
Published in
American Journal of Medical Genetics Part A
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