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Search Results - Chaabouni-Bouhamed, H.
Search Results - Chaabouni-Bouhamed, H.
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Update on the Genetics of Bardet-Biedl Syndrome
by
M'hamdi, O.
,
Ouertani, I.
,
Chaabouni-Bouhamed, H.
Published in
Molecular syndromology
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Mutation spectrum and prevalence of BRCA1 and BRCA2 genes in patients with familial and early-onset breast/ovarian cancer from Tunisia
by
Riahi, A.
,
Kharrat, M.
,
Ghourabi, M. E.
,
Khomsi, F.
,
Gamoudi, A.
,
Lariani, I.
,
May, A. E.
,
Rahal, K.
,
Chaabouni-Bouhamed, H.
Published in
Clinical genetics
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Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
by
Kelmemi, W
,
Teeuw, M E
,
Bochdanovits, Z
,
Ouburg, S
,
Jonker, M A
,
Alkuraya, F
,
Hashem, M
,
Kayserili, H
,
van Haeringen, A
,
Sheridan, E
,
Masri, A
,
Cobben, J M
,
Rizzu, P
,
Kostense, P J
,
Dommering, C J
,
Henneman, L
,
Bouhamed-Chaabouni, H
,
Heutink, P
,
Ten Kate, L P
,
Cornel, M C
Published in
BMC medical genetics
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RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian family
by
Chograni, Manèl
,
Alkuraya, Fowzan S
,
Maazoul, Faouzi
,
Lariani, Imen
,
Chaabouni-Bouhamed, Habiba
Published in
Investigative ophthalmology & visual science
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Tunisia: Communities and Community Genetics
by
Chaabouni-Bouhamed, Habiba
Published in
Community genetics
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Absence of PITX3 mutation in a Tunisian family with congenital cataract and mental retardation
by
Chograni, Manèl
,
Chaabouni, Myriam
,
Chelly, Imen
,
Helayem, Mohamed Bechir
,
Chaabouni-Bouhamed, Habiba
Published in
Molecular vision
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Mutation spectrum and prevalence of BRCA 1 and BRCA 2 genes in patients with familial and early‐onset breast/ovarian cancer from Tunisia
by
Riahi, A.
,
Kharrat, M.
,
Ghourabi, M. E.
,
Khomsi, F.
,
Gamoudi, A.
,
Lariani, I.
,
May, A. E.
,
Rahal, K.
,
Chaabouni‐Bouhamed, H.
Published in
Clinical genetics
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412 Combination of Genomic Technologies and Consanguinity in Order to Identify Pathogenic Variants in Recessive Disorders
by
Makrythanasis, P
,
Nelis, M
,
Santoni, FA
,
Guipponi, M
,
Béna, F
,
Vanier, A
,
Duriaux-Sail, G
,
Gimelli, S
,
Stathaki, E
,
Falconnet, E
,
Temtamy, S
,
Megarbane, A
,
Aglan, M
,
Zaki, M
,
Fokstuen, S
,
Bottani, A
,
Masri, A
,
Psoni, S
,
Kitsiou, S
,
Frissyra, H
,
Kanavakis, E
,
All-Allawi, N
,
Sefiani, A
,
Al-Hait, S
,
Elalaoui, S
,
Jalkh, N
,
Al-Gazali, L
,
Al-Jasmi, F
,
Bouhamed, H Chaabouni
,
Hamamy, H
,
Antonarakis, SE
Published in
Archives of disease in childhood
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