Houda Benailly-Karmous

Nice, France

Last Updated: 09/26/2026

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Found 11 publications

Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

Journal: Clinical genetics

Published: May 21, 2026

Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome.

Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome.

Journal: American journal of medical genetics. Part A

Published: May 16, 2022

EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder.

EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder.

Journal: Clinical genetics

Published: November 27, 2020

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

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

Journal: American journal of medical genetics. Part A

Published: March 26, 2019

Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty.

Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty.

Journal: Molecular genetics & genomic medicine

Published: August 16, 2018

FANCD2 functions as a critical factor downstream of MiTF to maintain the proliferation and survival of melanoma cells.

FANCD2 functions as a critical factor downstream of MiTF to maintain the proliferation and survival of melanoma cells.

Journal: Scientific reports

Published: March 18, 2016

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

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

Journal: American journal of medical genetics. Part A

Published: May 11, 2015

Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.

Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.

Journal: American journal of medical genetics. Part A

Published: April 13, 2014

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

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

Journal: American journal of medical genetics. Part A

Published: October 22, 2013

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

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

Journal: American journal of medical genetics. Part A

Published: October 12, 2012

Renal cell carcinoma and a constitutional t(11;22)(q23;q11.2): case report and review of the potential link between the constitutional t(11;22) and cancer.

Renal cell carcinoma and a constitutional t(11;22)(q23;q11.2): case report and review of the potential link between the constitutional t(11;22) and cancer.

Journal: Cancer genetics

Published: March 14, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026