Clinical utility gene card for: Gorlin syndrome--update 2013
about
Basal cell nevus syndrome (Gorlin-Goltz syndrome): genetic predisposition, clinical picture and treatment.Signs and genetics of rare cancer syndromes with gastroenterological features.Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.Multiple 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.
P2860
Clinical utility gene card for: Gorlin syndrome--update 2013
description
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Clinical utility gene card for: Gorlin syndrome--update 2013
@en
Clinical utility gene card for: Gorlin syndrome--update 2013
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label
Clinical utility gene card for: Gorlin syndrome--update 2013
@en
Clinical utility gene card for: Gorlin syndrome--update 2013
@nl
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Clinical utility gene card for: Gorlin syndrome--update 2013
@en
Clinical utility gene card for: Gorlin syndrome--update 2013
@nl
P2093
P2860
P50
P356
P1476
Clinical utility gene card for: Gorlin syndrome--update 2013
@en
P2093
Giovanna Bianchi Scarra
Lorenza Pastorino
Mima Situm
Sonja Levanat
P2860
P2888
P356
10.1038/EJHG.2012.299
P577
2013-01-30T00:00:00Z
P6179
1025632855