Publications by authors named "Labiba Adala"

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c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis.
Ameni Kdissa, Klaus Brusgaard, Mahdi Ksiaa, Lamia Golli, Olfa Hallara, Labiba Adala

Cancer Genet· January 2020

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Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.
Abdelbasset Amara, Labiba Adala, Ilhem Ben Charfeddine, Ons Mamaï, Amira Mili

Eur J Paediatr Neurol· March 2012

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Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.
Amira Mili, Ilhem Ben Charfeddine, Ons Mamaï, Sonia Abdelhak, Labiba Adala

J Hum Genet· March 2012

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Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.
Ilhem Ben Charfeddine, Felix G Riepe, Najoua Kahloul, Alexandra E Kulle, Labiba Adala

Gen Comp Endocrinol· February 2012

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An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation.
Moez Gribaa, Mohamed Younes, Yosra Bouyacoub, Wided Korbaa, Ilhem Ben Charfeddine, Labiba Adala

J Bone Miner Metab· March 2010

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