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Alain Verloes
Researcher at University of Paris
Publications - 464
Citations - 21574
Alain Verloes is an academic researcher from University of Paris. The author has contributed to research in topics: Microcephaly & Noonan syndrome. The author has an hindex of 73, co-authored 450 publications receiving 19231 citations. Previous affiliations of Alain Verloes include Institut Universitaire de France & Max Planck Society.
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Feingold syndrome: report of a new family and review.
TL;DR: The seventh family with Feingold syndrome is reported on, with a male infant with esophageal and duodenal atresia, brachymesophalangy of the fifth fingers, bilateral syndactyly of toes 4-5, and relative microcephaly, and facial anomalies.
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Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
TL;DR: Mental retardation with blepharo‐naso‐facial abnormalities and hand malformations: a new syndrome is diagnosed.
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Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies
Andrée Delahaye,Pierre Bitoun,Séverine Drunat,Marion Gérard-Blanluet,Nicolas Chassaing,Annick Toutain,Alain Verloes,Alain Verloes,Frédérique Gatelais,Marie Legendre,Laurence Faivre,Sandrine Passemard,Sandrine Passemard,Azzedine Aboura,Sophie Kaltenbach,Samuel Quentin,Céline Dupont,Anne-Claude Tabet,Serge Amselem,Jacques Elion,Pierre Gressens,Pierre Gressens,Eva Pipiras,Eva Pipiras,Brigitte Benzacken +24 more
TL;DR: Results show that array-CGH provides a high diagnostic yield in patients with syndromal ODAs and can identify previously unknown chromosomal regions associated with these conditions and may help identify genes involved in ocular development.
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Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases.
Aude Tessier,Mélie Sarreau,Fanny Pelluard,Gwenaëlle André,Sophie Blesson,Martine Bucourt,P. Dechelotte,Laurence Faivre,Thierry Frebourg,Alice Goldenberg,Valérie Goua,Corinne Jeanne-Pasquier,Fabien Guimiot,Annie Laquerrière,Nicole Laurent,Mathilde Lefebvre,Philippe Loget,Martine Maréchaud,Charlotte Mechler,Marie-Josée Perez,J.C. Sabourin,Alain Verloes,Sophie Patrier,Anne-Marie Guerrot +23 more
TL;DR: Fraser syndrome is a rare malformation recessive disorder with major criteria are cryptophtalmos, syndactyly, respiratory, genital and urinary tract anomalies.
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Brachymorphism-onychodysplasia-dysphalangism syndrome.
Alain Verloes,Dominique Bonneau,O Guidi,Michel Berthier,Denis Oriot,L. Van Maldergem,Lucien Koulischer +6 more
TL;DR: It is suggested that the pattern of anomalies presented by these children closely resembles a syndrome incompletely delineated in 1971 by Senior in six children, which has often been considered to be a mild form of Coffin-Siris syndrome, and is an independent entity (BOD syndrome).