- Frasier syndrome
Infobox_Disease
Name = PAGENAME
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DiseasesDB = 32455
ICD10 =
ICD9 =
ICDO =
OMIM = 136680
MedlinePlus =
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MeshID = D052159Frasier syndrome is a urogenital anomaly associated with
WT1 .cite journal |author=Klamt B, Koziell A, Poulat F, "et al" |title=Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms |journal=Hum. Mol. Genet. |volume=7 |issue=4 |pages=709–14 |year=1998 |month=April |pmid=9499425 |doi= |url=http://hmg.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=9499425]It was first characterized in 1964.cite journal |author=FRASIER SD, BASHORE RA, MOSIER HD |title=GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS |journal=J. Pediatr. |volume=64 |issue= |pages=740–5 |year=1964 |month=May |pmid=14149008 |doi= |url=]
References
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