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Emna Kerkeni

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Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|September 11, 2014

Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean regionSana Hsouna, Nizar Ben Halim, Khaled Lasram, et al.

Annals of Human Genetics|April 5, 2013

A novel mutation in FGD4/FRABIN causes Charcot Marie Tooth disease type 4H in patients from a consanguineous Tunisian familyChokri Boubaker, Inès Hsairi-Guidara, Christel Castro, et al.

BMC Pediatrics|August 31, 2018

Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndromeNehla Ghedira, Arnaud Lagarde, Karim Ben Ameur, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 23 results.

Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|September 11, 2014

Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean regionSana Hsouna, Nizar Ben Halim, Khaled Lasram, et al.

Annals of Human Genetics|April 5, 2013

A novel mutation in FGD4/FRABIN causes Charcot Marie Tooth disease type 4H in patients from a consanguineous Tunisian familyChokri Boubaker, Inès Hsairi-Guidara, Christel Castro, et al.

BMC Pediatrics|August 31, 2018

Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndromeNehla Ghedira, Arnaud Lagarde, Karim Ben Ameur, et al.

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