Publications by authors named "Houda Karmous-Benailly"

13Publications

Prenatal diagnosis of micrognathia in 41 fetuses: Retrospective analysis of outcome and genetic etiologies.

Am J Med Genet A 2019 12 11;179(12):2365-2373. Epub 2019 Sep 11.

Hôpital de la Timone, Medical Genetics, Marseille, Provence-Alpes-Côte d'Azur, France.

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http://dx.doi.org/10.1002/ajmg.a.61359DOI Listing
December 2019

Neurodevelopmental and immunological features in a child presenting 22q13.2 microdeletion.

Am J Med Genet A 2016 Mar 14;170(3):792-4. Epub 2015 Nov 14.

University Department of Child and Adolescent Psychiatry, Nice Children's Hospitals CHU-Lenval, Nice, France.

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http://dx.doi.org/10.1002/ajmg.a.37470DOI Listing
March 2016

De novo 4q duplication/deletion in a fetus with a congenital heart defect.

Am J Med Genet A 2015 Aug 19;167A(8):1932-6. Epub 2015 Jun 19.

Service de Génétique Médicale, Hôpital de l'Archet II, St Antoine de Ginestière, France.

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http://dx.doi.org/10.1002/ajmg.a.37005DOI Listing
August 2015

Delineation of a region responsible for panhypopituitarism in 20p11.2.

Am J Med Genet A 2013 Jul 8;161A(7):1547-54. Epub 2013 May 8.

Service de Génétique Médicale, Hôpital de l'Archet II, CHU Nice, Nice Cedex 3, France.

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http://dx.doi.org/10.1002/ajmg.a.35921DOI Listing
July 2013

Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.

Eur J Med Genet 2006 Sep-Oct;49(5):431-8. Epub 2006 Feb 10.

Service de génétique médicale, hôpital l'Archet 2, CHU de Nice, 151, route de Saint-Antoine-de-Ginestière, 06202 Nice cedex 03, France.

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http://dx.doi.org/10.1016/j.ejmg.2006.01.008DOI Listing
November 2006

Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?

Prenat Diagn 2005 Mar;25(3):193-7

Service de Biologie du Développement, Hôpital Robert Debré, Paris, France.

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http://dx.doi.org/10.1002/pd.1102DOI Listing
March 2005