Interstitial deletion of 13q22?q31: Case report and review of the literature

Morales,  J.A.; Mendizabal,  A.P.; Vasquez,  A.I.; Figuera,  L.E.; Gonzalez-Garcia,  J.R.

Review

Fecha

2006

Registro en:

http://www.scopus.com/inward/record.url?eid=2-s2.0-33748201593&partnerID=40&md5=61a1ccb85a34b6689ff400118c9a1877

http://hdl.handle.net/20.500.12104/42345

10.1097/01.mcd.0000204990.46743.7b

https://repositorioslatinoamericanos.uchile.cl/handle/2250/7251078

Autor

Morales, J.A.

Mendizabal, A.P.

Vasquez, A.I.

Figuera, L.E.

Gonzalez-Garcia, J.R.

Institución

Universidad de Guadalajara (México)

Resumen

In the present study we describe a patient with characteristic brachydactily, developmental delay and interstitial del 13q22?q31. After the review of the literature, few cases sharing similar chromosomal deletions were found and they displayed little resemblance with our patient. We discuss the phenotype correlation among the deleted regions in such cases. � 2006 Lippincott Williams & Wilkins, Inc.

Materias

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