Condition: Cerebral Palsy


rs1553630279 in CTNNB1 gene and Cerebral Palsy PMID 27915094 2017 Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.

PMID 24668549 2014 A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.

PMID 2614104 1989 [Intraoperative echocardiographic assessment of left ventricular muscle volume changes after intracardiac operation under cardiopulmonary bypass].

rs28934906 in MECP2 gene and Cerebral Palsy PMID 19722030 2009 Genotype-phenotype correlation in Brazillian Rett syndrome patients.

PMID 12065946 2003 Prenatal diagnosis in Rett syndrome.

PMID 10944834 2000 Chronic osteomyelitis in patients with sickle cell disease.

PMID 20031356 2010 Identification and characterization of novel sequence variations in MECP2 gene in Rett syndrome patients.

PMID 17089071 2007 MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome.

PMID 17881312 2008 Homozygosity for MECP2 gene in a girl with classical Rett syndrome.