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1.
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
Indian J Hum Genet
; 19(3): 331-6, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-24339547
2.
RETRACTED: Gradual emergence followed by exponential spread of the SARS-CoV-2 Omicron variant in Africa.
Science
; 378(6623): eadd8737, 2022 12 02.
Article
in English
| MEDLINE | ID: mdl-36454863
3.
Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.
J Community Health
; 36(6): 943-8, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-21442339
4.
Retraction.
Science
; 378(6626): 1284-1285, 2022 Dec 23.
Article
in English
| MEDLINE | ID: mdl-36537892
5.
Prevalence of the Aurora kinase C c.144delC mutation in infertile Moroccan men.
Fertil Steril
; 101(4): 1086-90, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-24484996
6.
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.
Gene
; 523(1): 103-5, 2013 Jul 01.
Article
in English
| MEDLINE | ID: mdl-23590985
7.
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.
Arch Dermatol Res
; 305(1): 53-57, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23143338
8.
Association of the MTHFR A1298C variant with unexplained severe male infertility.
PLoS One
; 7(3): e34111, 2012.
Article
in English
| MEDLINE | ID: mdl-22457816
9.
Association of spermatogenic failure with the b2/b3 partial AZFc deletion.
PLoS One
; 7(4): e34902, 2012.
Article
in English
| MEDLINE | ID: mdl-22514689
10.
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
Indian J Hum Genet
; 2013 July-Sept ;19 (3): 331-336
Article
in English
| IMSEAR | ID: sea-156586
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