NBCCS secondary to an interstitial chromosome 9q deletion.
about
Nevoid basal cell carcinoma syndrome (Gorlin syndrome)9q22 Deletion--first familial case.PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French studyMultiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay
P2860
NBCCS secondary to an interstitial chromosome 9q deletion.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年學術文章
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name
NBCCS secondary to an interstitial chromosome 9q deletion.
@en
NBCCS secondary to an interstitial chromosome 9q deletion.
@nl
type
label
NBCCS secondary to an interstitial chromosome 9q deletion.
@en
NBCCS secondary to an interstitial chromosome 9q deletion.
@nl
prefLabel
NBCCS secondary to an interstitial chromosome 9q deletion.
@en
NBCCS secondary to an interstitial chromosome 9q deletion.
@nl
P2093
P2860
P1476
NBCCS secondary to an interstitial chromosome 9q deletion.
@en
P2093
P2860
P304
P356
10.1111/J.1365-2230.2004.01590.X
P577
2004-09-01T00:00:00Z