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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
Zied Riahi
,
Crystel Bonnet
,
Rim Zainine
,
Malek Louha
,
Yosra Bouyacoub
,
et al.
Journal articles
pasteur-01060192v1
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Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism
Rahma Mkaouar
,
Lamia Cherif Ben Abdallah
,
Chokri Naouali
,
Saida Lahbib
,
Zinet Turki
,
et al.
Journal articles
pasteur-03521812v1
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A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD
Yassine Naasse
,
Amina Bakhchane
,
Hicham Charoute
,
Farida Jennane
,
Joelle Bignon-Topalovic
,
et al.
Journal articles
pasteur-03521891v1
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Specific aspects of consanguinity: some examples from the tunisian population.
Lilia Romdhane
,
Nizar Ben Halim
,
Insaf Rejeb
,
Rym Kefi
,
Yosra Bouyacoub
,
et al.
Journal articles
pasteur-01061190v1
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Identification of a novel mutation of LAMB3 gene in a lybian patient with hereditary epidermolysis bullosa by whole exome sequencing
N. Laroussi
,
O. Messaoud
,
M. Chargui
,
C.B. Fayala
,
A. Elahlafi
,
et al.
Journal articles
hal-01534741v1
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Y-chromosome AZFc structural architecture and relationship to male fertility
Celia Ravel
,
Sandra Chantot-Bastaraud
,
Brahim El Houate
,
Hassan Rouba
,
Marie Legendre
,
et al.
Journal articles
inserm-04133897v1
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