A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent Müllerian duct syndrome.
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Gonadal and sex differentiation abnormalities of dogs and catsRNA-Seq approach for genetic improvement of meat quality in pig and evolutionary insight into the substrate specificity of animal carbonyl reductases.Coincidence of Persistent Müllerian duct syndrome and testicular tumors in dogsA molecular diagnostic test for persistent Müllerian duct syndrome in miniature schnauzer dogs.Disorder of sexual development in a Yorkshire terrier (78, XY; SRY-positive).Surveyor assay to diagnose persistent Müllerian duct syndrome in Miniature Schnauzers.XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris).Prevalence of the AMHR2 mutation in Miniature Schnauzers and genetic investigation of a Belgian Malinois with persistent Müllerian duct syndrome.Sequence variations in equine candidate genes For XX and XY inherited disorders of sexual development.
P2860
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P2860
A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent Müllerian duct syndrome.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
A single base pair mutation en ...... stent Müllerian duct syndrome.
@en
type
label
A single base pair mutation en ...... stent Müllerian duct syndrome.
@en
prefLabel
A single base pair mutation en ...... stent Müllerian duct syndrome.
@en
P2093
P2860
P1433
P1476
A single base pair mutation en ...... stent Müllerian duct syndrome.
@en
P2093
Donald H Schlafer
Mark E Haskins
Shashikant Pujar
Shengqin Wan
Vicki N Meyers-Wallen
Xiufeng Wu
P2860
P356
10.2164/JANDROL.108.005736
P50
P577
2008-08-21T00:00:00Z