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Lilia Kraoua

Showing results (1-10 of 28) with videos related to

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International Journal of Molecular Sciences|February 25, 2023
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic CardiomyopathyStéphane Zaffran, Lilia Kraoua, Hager Jaouadi
American Journal of Medical Genetics. Part A|July 20, 2012
Pseudoaminopterin syndromeLilia Kraoua, Yline Capri, Laurence Perrin, et al.
Annales D'Endocrinologie|December 19, 2016
Partial hypopituitarism in a female patient with a 45,X/46,XY mosaicismIbtissem Oueslati, Lilia Kraoua, Karima Khiari, et al.
American Journal of Medical Genetics. Part A|October 28, 2010
Germinal mosaicism in Noonan syndrome: A family with two affected siblings of normal parentsSiham Chafai Elalaoui, Lilia Kraoua, Céline Liger, et al.
Birth Defects Research|January 20, 2026
First Detection of 1p36 Deletion by Whole-Exome Sequencing in a Tunisian PatientNesrine Kerkeni, Maher Kharrat, Lilia Kraoua, et al.
La Tunisie Medicale|September 17, 2024
Nadia Ben Amor, Lilia Kraoua, Rahma Damak, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Constitutional NRAS mutations are rare among patients with Noonan syndrome or juvenile myelomonocytic leukemiaLilia Kraoua, Hubert Journel, Philippe Bonnet, et al.
European Journal of Medical Genetics|February 15, 2011
A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardationImen Rejeb, Lamia Ben Jemaa, Leila Abaied, et al.
European Journal of Medical Genetics|November 13, 2012
Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategyMediha Trabelsi, Imen Chelly, Faouzi Maazoul, et al.
European Journal of Medical Genetics|May 31, 2011
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case reportLilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
International Journal of Molecular Sciences|February 25, 2023
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic CardiomyopathyStéphane Zaffran, Lilia Kraoua, Hager Jaouadi
American Journal of Medical Genetics. Part A|July 20, 2012
Pseudoaminopterin syndromeLilia Kraoua, Yline Capri, Laurence Perrin, et al.
Annales D'Endocrinologie|December 19, 2016
Partial hypopituitarism in a female patient with a 45,X/46,XY mosaicismIbtissem Oueslati, Lilia Kraoua, Karima Khiari, et al.
American Journal of Medical Genetics. Part A|October 28, 2010
Germinal mosaicism in Noonan syndrome: A family with two affected siblings of normal parentsSiham Chafai Elalaoui, Lilia Kraoua, Céline Liger, et al.
Birth Defects Research|January 20, 2026
First Detection of 1p36 Deletion by Whole-Exome Sequencing in a Tunisian PatientNesrine Kerkeni, Maher Kharrat, Lilia Kraoua, et al.
La Tunisie Medicale|September 17, 2024
Nadia Ben Amor, Lilia Kraoua, Rahma Damak, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Constitutional NRAS mutations are rare among patients with Noonan syndrome or juvenile myelomonocytic leukemiaLilia Kraoua, Hubert Journel, Philippe Bonnet, et al.
European Journal of Medical Genetics|February 15, 2011
A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardationImen Rejeb, Lamia Ben Jemaa, Leila Abaied, et al.
European Journal of Medical Genetics|November 13, 2012
Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategyMediha Trabelsi, Imen Chelly, Faouzi Maazoul, et al.
European Journal of Medical Genetics|May 31, 2011
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case reportLilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, et al.
Pageof 3