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Wide clinical spectrum in Zimmermann-Laband syndrome
(2011)
Gingival fibromatosis can be present as an isolated form or be part of a genetic disease. The Zimmermann-Laband syndrome (ZLS) is a rare disorder inherited as an autosomal dominant fashion, clinically characterized by ...
Wide clinical spectrum in Zimmermann-Laband syndrome
(2011)
Gingival fibromatosis can be present as an isolated form or be part of a genetic disease. The Zimmermann-Laband syndrome (ZLS) is a rare disorder inherited as an autosomal dominant fashion, clinically characterized by ...
A de novo interstitial 6q deletion in a boy with a split hand malformation
(2007)
We report on a de novo interstitial deletion of (6)(q15q22.2) in a 5-year-old boy with developmental delay, microcephaly, facial dysmorphism, cryptorchidism, congenital heart defect, and split-hand malformation. Previous ...
Sistema de seguimiento y control de pacientes, caso: Instituto de Genética
(2009-09-04)
El Instituto de Genética es una Unidad Académica, de servicios e investigación, encargada de planificar, ejecutar y evaluar programas y proyectos de investigación y desarrollo científico en el campo de la genética humana. ...
Sistema de seguimiento y control de pacientes, caso: Instituto de Genética
(2009-09-04)
El Instituto de Genética es una Unidad Académica, de servicios e investigación, encargada de planificar, ejecutar y evaluar programas y proyectos de investigación y desarrollo científico en el campo de la genética humana. ...
Effect of ZNF217 gene polymorphisms on colorectal cancer development in a Mexican population
(2015)
The ZNF217 gene, a potential oncogene amplified and overexpressed in several cancers including colorectal cancer (CRC), acts as a transcription factor that activates or represses target genes. The polymorphisms rs16998248 ...
Effect of ZNF217 gene polymorphisms on colorectal cancer development in a Mexican population
(2015)
The ZNF217 gene, a potential oncogene amplified and overexpressed in several cancers including colorectal cancer (CRC), acts as a transcription factor that activates or represses target genes. The polymorphisms rs16998248 ...
Benign familial macrocephaly in a mother-son pair
(2010)
Benign familial macrocephaly in a mother-son pair: Macrocephaly can be found isolated or associated with other anomalies as a part of specific syndrome. Benign Familial Macrocephaly (BFM) is a primary macrocephaly and ...
Benign familial macrocephaly in a mother-son pair
(2010)
Benign familial macrocephaly in a mother-son pair: Macrocephaly can be found isolated or associated with other anomalies as a part of specific syndrome. Benign Familial Macrocephaly (BFM) is a primary macrocephaly and ...