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1 . Academic Journal
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array
저자
by
Elidrissi Errahhali, Manal
;
Elidrissi Errahhali, Mounia
;
Ramdani, Sara
;
Lhousni, Saida
;
Benajiba, Noufissa
, et al.
소스
In
Archives de pédiatrie
February 2024 31(2):112-116
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7 . Academic Journal
Novel variant in Moroccan patient with hereditary spastic paraplegia type 35
저자
by
Sifeddine, Najat
;
Amalou, Ghita
;
Bouzidi, Aymane
;
Charif, Majida
;
Nahili, Halima
, et al.
소스
In
Human Gene
December 2023 38
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7 . Academic Journal
A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias
저자
by
Lhousni, Saida
;
Charif, Majida
;
Derouich, Yassine
;
Elidrissi Errahhali, Mounia
;
Elidrissi Errahhali, Manal
, et al.
소스
In
Bone
October 2023 175
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7 . Academic Journal
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders
저자
by
Langhammer, Franziska
;
Maroofian, Reza
;
Badar, Rueda
;
Gregor, Anne
;
Rochman, Michelle
, et al.
소스
In
Genetics in Medicine
August 2023 25(8)
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7 . Academic Journal
First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta
저자
by
Nouara, Falah
;
Amalou, Ghita
;
Bouzidi, Aymane
;
Charif, Majida
;
Charoute, Hicham
, et al.
소스
In
Archives of Oral Biology
October 2022 142
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7 . Academic Journal
Syndromic Hearing Loss in Moroccan families is associated to homozygous missense variants in COL4A3 and MASP1
저자
by
Amalou, Ghita
;
Aitraise, Imane
;
Bouzidi, Aymane
;
Essadssi, Soukaina
;
Charif, Majida
, et al.
소스
In
Human Gene
September 2022 33
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7 . Academic Journal
A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability
저자
by
Krami, Al Mehdi
;
Bouzidi, Aymane
;
Charif, Majida
;
Amalou, Ghita
;
Charoute, Hicham
, et al.
소스
In
European Journal of Medical Genetics
June 2022 65(6)
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7 . Academic Journal
Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
저자
by
Salime, Sara
;
Charif, Majida
;
Bousfiha, Amale
;
Elrharchi, Soukaina
;
Bakhchane, Amina
, et al.
소스
In
International Journal of Pediatric Otorhinolaryngology
October 2017 101:25-29
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7 . Academic Journal
Population structure and genetic diversity of Moroccan cannabis (Cannabis sativa L.) germplasm through simple sequence repeat (SSR) analysis.
저자
by
Benkirane, Chaymae
;
Charif, Majida
;
Müller, Christina M.
;
Taaifi, Yassine
;
Mansouri, Farid
, et al.
소스
Genetic Resources & Crop Evolution; Jun2024, Vol. 71 Issue 5, p2037-2051, 15p
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7 . Academic Journal
Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss
저자
by
Bakhchane, Amina
;
Bousfiha, Amale
;
Charoute, Hicham
;
Salime, Sara
;
Detsouli, Mustapha
, et al.
소스
In
European Journal of Medical Genetics
June 2016 59(6-7):325-329
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