Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome.
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Clinical and genetic characterization of basal cell carcinoma and breast cancer in a single patientEarly diagnosis of Gorlin-Goltz syndrome: case report9q22 Deletion--first familial case.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.Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay
P2860
Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 21 February 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Early detection of chromosome ...... basal cell carcinoma syndrome.
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Early detection of chromosome ...... basal cell carcinoma syndrome.
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type
label
Early detection of chromosome ...... basal cell carcinoma syndrome.
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Early detection of chromosome ...... basal cell carcinoma syndrome.
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prefLabel
Early detection of chromosome ...... basal cell carcinoma syndrome.
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Early detection of chromosome ...... basal cell carcinoma syndrome.
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P2093
P1476
Early detection of chromosome ...... basal cell carcinoma syndrome.
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P2093
Joris R Vermeesch
Katleen Ballon
Koen Devriendt
Liliane Ameye
Martine Borghgraef
Thomy J L de Ravel
P304
P356
10.1016/J.EJMG.2009.02.002
P577
2009-02-21T00:00:00Z