Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

8 Oct 2018

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Pluripotent Stem Cells Research
Share to Renal and related cancers
Share to Reproductive Biology and Fertility

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30297906
DOI: 10.1038/s41431-018-0283-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertilityPMID 30297906Read ↗

TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization FailureSemantic proximity Read ↗

The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility.Semantic proximity Read ↗

Novel variants in TUBB8 gene cause multiple phenotypic abnormalities in human oocytes and early embryos.Semantic proximity Read ↗

Three Novel Mutations in TUBB8 Cause Female Infertility Due to Multiple Morphological Abnormalities of the Oocyte and Early Embryo.Semantic proximity Read ↗

Genetic screening and analysis of TUBB8 variants in females seeking ART.Semantic proximity Read ↗

Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defects.Semantic proximity Read ↗

Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations.Semantic proximity Read ↗

Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations.Semantic proximity Read ↗

Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development.Semantic proximity Read ↗

A novel compound heterozygous mutation in TUBB8 causing early embryonic developmental arrest.Semantic proximity Read ↗

Identification of novel variants and expansion of the phenotypic spectrum in PATL2, WEE2, and TUBB8 associated with human early embryonic arrest.Semantic proximity Read ↗

Identification of TUBB8 Variants in 5 Primary Infertile Women with Multiple Phenotypes in Oocytes and Early Embryos.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.