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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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Journal Article
Ring chromosome 9 in a newborn male presenting with facial dysmorphia, hypospadias and skeletal abnormalities.
TL;DR: A newborn male presenting with a peculiar appearance, hypertonia, a flexum attitude, hypospadias and skeletal abnormalities was found to bear a r 9 chromosome and a phenotypic distinction between late presenting forms is discussed.
Journal ArticleDOI
Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: New cases of “polyvalvular heart disease syndrome” or new association?
Thomas Edouard,Catherine Prost-Squarcioni,Yves Dulac,Frédéric Vaysse,Hélène Cavé,Pascale Saugier-Veber,Georges Bourrouillou,Alain Verloes,Maithé Tauber,Eric Bieth +9 more
TL;DR: Five cases in two unrelated families with the same association of polyvalvular heart disease, distinctive facial appearance, and, except the father in family 2, major joint hypermobility are reported, suggesting a connective tissue disorder different from Marfan syndrome or Ehlers-Danlos syndrome.
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Absence of microcephalin gene mutations in a large cohort of non-consanguineous patients with autosomal recessive primary microcephaly.
Iris Scala,Luigi Titomanlio,Ennio Del Giudice,Sandrine Passemard,Chiara Figliuolo,Patrizia Annunziata,Barbara Granese,Elena Scarpato,Alain Verloes,Generoso Andria +9 more
TL;DR: Absence of Microcephalin Gene Mutations in a Large Cohort of Non-Consanguineous Patients With Autosomal Recessive Primary MicrocePHaly is confirmed.
Journal Article
Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome?
Alain Verloes,Yves Gillerot,J. Delfortrie,Zeevaert-Arnold Mt,Collard R,Lucien Koulischer,J. P. Fryns +6 more
TL;DR: Two sibs with an undescribed MCA/MR syndrome have a 46,XY chromosome constitution and the first patient is profoundly mentally retarded, and the general aspect of the propositus clearly resembles Borjeson-Forssman-Lehmann syndrome.