Suchergebnisse - "Gourabi, Hamid"

PubPharm (6)

1

Novel cause of hereditary obstructive azoospermia : a T2 allele in the CFTR gene

enthalten in: Reproductive biomedicine online | 2009

von Radpour, R. | Taherzadeh-Fard, E. | Gourabi, H. | +3

2

Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility

enthalten in: Journal of andrology | 2008

von Radpour, R. | Gourabi, H. | Dizaj, A. | +2

3

Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype

enthalten in: Journal of andrology | 2008

von Radpour, R. | Gourabi, H. | Gilani, M. | +1

4

Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens

enthalten in: Journal of andrology | 2007

von Radpour, R. | Gourabi, H. | Gilani, M. | +1

5

Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens

enthalten in: Molecular human reproduction | 2006

von Radpour, R. | Gourabi, H. | Gilani, M. | +3

6

Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens

enthalten in: Molecular human reproduction | 2006

von Radpour, R. | Gilani, M. | Gourabi, H. | +2

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