t/gene-chd7

CHD7 gene

Discuss publications and research concerning the CHD7 gene.

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Related literature

[Clinical phenotype and genetic analysis of 7 neonates with CHARGE syndrome caused by CHD7 gene variants].
CHD7
Exome Sequencing Studies in Syndromic Patients With Cleft Lip and/or Palate: Systematic Review.
CHD7
Differential Transcriptome Analysis of Intrauterine UPD6pat Fetuses With Distinct Phenotypes.
CHD7
Novel Protein-Altering Variants in Cleft Genes Transmitted in Families With NSCL±P.
CHD7
Generation of induced pluripotent stem cells from a patient with CHARGE syndrome with athymia, harboring a heterozygous mutation in CHD7.
CHD7
[Kallmann syndrome in a girl caused by a novel CHD7 variant].
CHD7
Novel KISS1 Gene Mutation Leading to Male Hypogonadotropic Hypogonadism.
CHD7
New CHARGE Syndrome Mouse Models Reveal the Contribution of the Enzymatic Activity of CHD7 in Pathogenesis.
CHD7
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome.
CHD7
KMT2C Polymorphism in Familial Hypospadias.
CHD7

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