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Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene
by
Chouk, Hamza
,
Ben Rejeb, Mohamed
,
Boussofara, Lobna
,
Elmabrouk, Haїfa
,
Ghariani, Najet
,
Sriha, Badreddine
,
Saad, Ali
,
H'Mida, Dorra
,
Denguezli, Mohamed
Published in
Human genomics
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X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
by
Chouk, Hamza
,
Saad, Sarra
,
Dimassi, Sarra
,
Fetoui, Nadia Ghariani
,
Bennour, Ayda
,
Gammoudi, Rima
,
Elmabrouk, Haifa
,
Saad, Ali
,
Denguezli, Mohamed
,
H'mida, Dorra
Published in
BMC medical genomics
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Unusual facial lesions in H syndrome
by
Rekik, Mariem
,
Bahloul, Emna
,
Ben Rejeb, Mohamed
,
Sellami, Khadija
,
Charfi, Slim
,
Chouk, Hamza
,
Boudaouara, Tahya
,
Turki, Hamida
Published in
Clinical case reports
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Is Tunisia ready for precision medicine? Challenges of medical genomics within a LMIC healthcare system
by
Trabelsi, Narjes
,
Othman, Houcemeddine
,
Bedhioufi, Hafsi
,
Chouk, Hamza
,
El Mabrouk, Haïfa
,
Mahdouani, Marwa
,
Gribaa, Moez
,
Saad, Ali
,
H’mida, Dorra
Published in
Journal of community genetics
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