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Page 1
Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population.
J Med Life. 2021 Nov-Dec;14(6):841-846. doi: 10.25122/jml-2021-0152.
J Med Life. 2021.
PMID: 35126756
Free PMC article.
Prevalence of Y chromosome microdeletion in azoospermic infertile males of Iraqi population.
Al-Janabi AM, Rahim AIR, Faris SA, Al-Khafaji SM, Jawad D.
Al-Janabi AM, et al. Among authors: al khafaji sm.
J Genet. 2020;99(0):18.
J Genet. 2020.
PMID: 32366729
Free article.
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The role of Y chromosome C-band size polymorphism in male infertility with a reference to their effect on the total length of the chromosome.
Yasseen AA, Al-Khafaji SM.
Yasseen AA, et al. Among authors: al khafaji sm.
Saudi Med J. 2004 Apr;25(4):452-5.
Saudi Med J. 2004.
PMID: 15083214
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The significance of autosomal C-band size polymorphism in male infertility.
Yasseen AA, Al-Khafaji SM.
Yasseen AA, et al. Among authors: al khafaji sm.
Saudi Med J. 2002 Dec;23(12):1473-7.
Saudi Med J. 2002.
PMID: 12518195
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Specific chromosomal satellite association among infertile male patients.
Yasseen AA, Al-Khafaji SM.
Yasseen AA, et al. Among authors: al khafaji sm.
Saudi Med J. 2004 Oct;25(10):1527-9.
Saudi Med J. 2004.
PMID: 15494850
No abstract available.
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