The molecular genetics of male infertility

scientific article

The molecular genetics of male infertility is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1093/MOLEHR/3.5.419
P698PubMed publication ID9239727
P5875ResearchGate publication ID13979614

P2093author name stringHorst J
Meschede D
P433issue5
P921main subjectmolecular geneticsQ210506
P304page(s)419-430
P577publication date1997-05-01
P1433published inMolecular Human ReproductionQ15761794
P1476titleThe molecular genetics of male infertility.
P478volume3

Reverse relations

cites work (P2860)
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Q77572389Genetics and human reproduction
Q29347248Germinal Cell Aplasia in Kif18a Mutant Male Mice Due to Impaired Chromosome Congression and Dysregulated BubR1 and CENP-E
Q36917079In vitro spermatogenesis as a method to bypass pre-meiotic or post-meiotic barriers blocking the spermatogenetic process: genetic and epigenetic implications in assisted reproductive technology
Q38440120Initiative for standardization of reporting genetics of male infertility
Q36095006Intracytoplasmic injection of spermatozoa and spermatogenic cells: its biology and applications in humans and animals
Q37026034Microarray detection of Y chromosome deletions associated with male infertility.
Q78103169Microdeletions within the azoospermia factor subregions of the Y chromosome in patients with idiopathic azoospermia
Q34069947Mitochondrial DNA mutations and male infertility
Q38322581Novel mutations in calcium/calmodulin-dependent protein kinase IV (CAMK4) gene in infertile men.
Q44264458Screening for microdeletions on the long arm of chromosome Y in 53 infertile men.
Q73901791Seminal plasma characteristics as indicators of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in men with obstructive azoospermia
Q51913980TSEG-1, a novel member of histone H2A variants, participates in spermatogenesis via promoting apoptosis of spermatogenic cells.
Q57733066The TNP1 haplotype - GCG is associated with azoospermia

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