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Article

Identification by whole-exome sequencing of novel mutation c.64C > G in the BTK gene of a fetus with X-linked agammaglobulinemia.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology - 1 Jun 2015

Yang Y-D, Tang H, Li W, Zhu Y-X, Huang H, Yi X, Su Y, Zhou T-H

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Share to Agammaglobulinaemia Tyrosine Kinase
Share to Agammaglobulinemia
Share to Exome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, X-Linked

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Share to Pregnancy

Share to Protein-Tyrosine Kinases

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 25413018
DOI: 10.1002/uog.14738

Genes

BTK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Identification by whole-exome sequencing of novel mutation c.64C > G in the BTK gene of a fetus with X-linked agammaglobulinemia.PMID 25413018Read ↗

A deep intronic BTK variant underlies X-linked agammaglobulinemia.Semantic proximity Read ↗

Case Report: Whole exome sequencing identifies a novel frameshift insertion c.1325dupT (p.F442fsX2) in the tyrosine kinase domain of BTK gene in a young Indian individual with X-linked agammaglobulinemiaSemantic proximity Read ↗

The spectrum of mutations in Btk that cause X-linked agammaglobulinemia.Semantic proximity Read ↗

Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia.Semantic proximity Read ↗

Whole Genome Sequencing identifies novel structural variant in a large Indian family affected with X - linked agammaglobulinemiaSemantic proximity Read ↗

[Genetic study of an X-linked agammaglobulinemia pedigree caused by an BTK mutation].Semantic proximity Read ↗

Identification of 22 novel BTK gene variants in B cell deficiency with hypogammaglobulinemia.Semantic proximity Read ↗

Identification of four novel mutations in BTK from six Chinese families with X-linked agammaglobulinemia.Semantic proximity Read ↗

Spectrum of BTK gene mutations in Vietnamese patients with X-linked agammaglobulinemia.Semantic proximity Read ↗

Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemia.Semantic proximity Read ↗

Clinical features and mutational analysis of X-linked agammaglobulinemia patients in MalaysiaSemantic proximity Read ↗

Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015).Semantic proximity Read ↗

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