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1 . Periodical
High frequency of hotspotmutation in PTPN11gene among Moroccan patients with Noonan syndrome
저자
by
Ouboukss, Fatima
;
Adadi, Najlae
;
Amasdl, Saadia
;
Smaili, Wiam
;
Laarabi, Fatima Zahra
, et al.
소스
Journal of Applied Genetics; May 2024, Vol. 65 Issue: 2 p303-308, 6p
Web of Science
Scopus
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7 . Academic Journal
High frequency of hotspot mutation in PTPN11 gene among Moroccan patients with Noonan syndrome
저자
by
Ouboukss, Fatima
;
Adadi, Najlae
;
Amasdl, Saadia
;
Smaili, Wiam
;
Laarabi, Fatima Zahra
, et al.
소스
Journal of Applied Genetics
. 65(2):303-308
Web of Science
Scopus
JCR 저널정보
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7 . Academic Journal
Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report.
저자
by
El Kadiri, Youssef
;
Ratbi, Ilham
;
Laarabi, Fatima Zahra
;
Kriouile, Yamna
;
Sefiani, Abdelaziz
, et al.
소스
BMC Medical Genomics
. 4/21/2021, Vol. 14 Issue 1, p1-6. 6p.
Open Access (BioMed Central)
Web of Science
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7 . Academic Journal
A novel single variant in the MEFV gene causing Mediterranean fever and Behçet's disease: a case report.
저자
by
Zerkaoui, Maria
;
Laarabi, Fatima Zahra
;
Ajhoun, Yousra
;
Chkirate, Bouchra
;
Sefiani, Abdelaziz
.
소스
Journal of Medical Case Reports
. 3/1/2018, Vol. 12 Issue 1, p1-4. 4p.
Open Access (BioMed Central)
Scopus
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7 . Academic Journal
Further evidence of POP1 mutations as the cause of anauxetic dysplasia.
저자
by
Elalaoui, Siham Chafai
;
Laarabi, Fatima Zahra
;
Mansouri, Maria
;
Mrani, Nidal Alaoui
;
Nishimura, Gen
, et al.
소스
American Journal of Medical Genetics. Part A; Sep2016, Vol. 170A Issue 9, p2462-2465, 4p
Web of Science
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7 . Academic Journal
AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population.
저자
by
Boualla, Lamiae
;
Tajir, Mariam
;
Oulahiane, Najat
;
Lyahyai, Jaber
;
Laarabi, Fatima Zahra
, et al.
소스
Genetic Testing & Molecular Biomarkers
. Nov2015, Vol. 19 Issue 11, p623-628. 6p.
Web of Science
Scopus
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7 . Academic Journal
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
저자
by
Jaouad, Imane Cherkaoui
;
El Alloussi, Mustapha
;
El alaoui, Siham Chafai
;
Laarabi, Fatima Zahra
;
Lyahyai, Jaber
, et al.
소스
BMC Oral Health; 2015, Vol. 15 Issue 1, p1-4, 4p
Open Access (BioMed Central)
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7 . Academic Journal
Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1 variants in Moroccan population
저자
by
Guaoua, Soukaina
;
Ratbi, Ilham
;
Laarabi, Fatima Zahra
;
Elalaoui, Siham Chafai
;
Jaouad, Imane Cherkaoui
, et al.
소스
BMC GENETICS
; DEC 29 2014, 15 p156 6p.
Open Access (BioMed Central)
Scopus
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7 . Academic Journal
Low Level of Consanguinity in Moroccan Families at High Risk of Breast Cancer
저자
by
Elalaoui, Siham Chafai
;
Jaouad, Imane Cherkaoui
;
Laarabi, Fatima Zahra
;
Elgueddari, Brahim El Khalil
;
Benjaafar, Noureddine
, et al.
소스
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION
; 2013, 14 2, p723-p726, 4p.
Scopus
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7 . Academic Journal
Frequencies of CYP3A5*1/*3 Variants in a Moroccan Population and Effect on Tacrolimus Daily Dose Requirements in Renal Transplant Patients
저자
by
Elmachad, Mustapha
;
Elkabbaj, Driss
;
Elkerch, Fatiha
;
Laarabi, Fatima Zahra
;
Barkat, Amina
, et al.
소스
GENETIC TESTING AND MOLECULAR BIOMARKERS
; JUN 2012, 16 6, p644-p647, 4p.
Scopus
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