Pages that link to "Q54565606"

The following pages link to Frequency of Y chromosome microdeletions and chromosomal abnormalities in infertile Thai men with oligozoospermia and azoospermia. (Q54565606):

Displaying 20 items.

• Male infertility in China: laboratory finding for AZF microdeletions and chromosomal abnormalities in infertile men from Northeastern China (Q34070167) (← links)
• Association of spermatogenic failure with the b2/b3 partial AZFc deletion (Q34238802) (← links)
• Molecular and cytogenetic studies of 101 infertile men with microdeletions of Y chromosome in 1,306 infertile Korean men (Q36016207) (← links)
• Cytogenetic abnormalities in 222 infertile men with azoospermia and oligospermia in Iran: Report and review (Q36377786) (← links)
• Detection of Y Chromosome Microdeletion is Valuable in the Treatment of Patients With Nonobstructive Azoospermia and Oligoasthenoteratozoospermia: Sperm Retrieval Rate and Birth Rate (Q36632615) (← links)
• High prevalence of genetic abnormalities in Middle Eastern patients with idiopathic non-obstructive azoospermia (Q36966504) (← links)
• Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey (Q36995764) (← links)
• Y chromosome microdeletions in sperm DNA of infertile patients from Tamil Nadu, south India (Q37197821) (← links)
• Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males (Q37641028) (← links)
• Relevance of genetic investigation in male infertility. (Q38181427) (← links)
• Male infertility in Northeast China: a cytogenetic study of 135 patients with non-obstructive azoospermia and severe oligozoospermia (Q40198747) (← links)
• The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men. (Q41950200) (← links)
• Cytogenetic abnormalities detected in patients with non-obstructive azoospermia and severe oligozoospermia (Q42909132) (← links)
• Fluorescence in situ hybridisation analysis of sex chromosome in non-obstructive azoospermic men. (Q43965016) (← links)
• Analysis of Y chromosome microdeletion in 1738 infertile men from northeastern China (Q45346061) (← links)
• Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience (Q47903641) (← links)
• Mild androgen insensitivity syndrome (MAIS): the identification of c.1783C>T mutation in two unrelated infertile men. (Q48058787) (← links)
• Testicular gene expression in cryptorchid boys at risk of azoospermia. (Q54382772) (← links)
• Comprehensive Genomic Study in Patients with Idiopathic Azoospermia and Oligoasthenoteratozoospermia (Q58050560) (← links)
• High frequency of microdeletion in TTY2 gene family in peripheral blood leukocytes of non-obstructive azoospermia patients (Q92761199) (← links)