Discover Community Create You

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

Genotyping and prenatal diagnosis of a large spinocerebellar ataxia pedigree in northeastern China.

Journal of genetics - 1 Aug 2011

Cao Dong-Hua, Liu Xiao-Li, Qiu Guang-Bin

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 Abortion, Eugenic
Share to Amniocentesis
Share to Ataxin-3
Share to Nerve Tissue Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nuclear Proteins

Share to Pregnancy

Share to Repressor Proteins

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 21869492
DOI: 10.1007/s12041-011-0090-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotyping and prenatal diagnosis of a large spinocerebellar ataxia pedigree in northeastern China.PMID 21869492Read ↗

Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South ChinaSemantic proximity Read ↗

[Molecular and prenatal diagnosis of a pedigree with spinocerebellar ataxia].Semantic proximity Read ↗

Prenatal Diagnosis of Severe Mitochondrial Diseases Caused by Nuclear Gene Defects: A Study in Japan Semantic proximity Read ↗

Clinical manifestation, imaging, and genotype analysis of two pedigrees with spinocerebellar ataxia.Semantic proximity Read ↗

Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan.Semantic proximity Read ↗

[Clinical features and genetic analysis of two Chinese pedigrees affected with Joubert syndrome].Semantic proximity Read ↗

Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individualsSemantic proximity Read ↗

Prenatal diagnosis of Friedreich ataxia.Semantic proximity Read ↗

[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with N-acetylglutamate synthase deficiency].Semantic proximity Read ↗

High-Resolution Haplotyping of the PAH Gene Enables Early Gestation Noninvasive Prenatal Diagnosis of Phenylketonuria and Evolution Analysis of Recurrent Pathogenic Variations.Semantic proximity Read ↗

Newborn mass screening and molecular genetics of phenylketonuria in east Asia.Semantic proximity Read ↗

Preimplantation Genetic Testing of Spinocerebellar Ataxia Type 2-Robust Tools for Direct and Indirect Detection of the ATXN2 CAG Repeat Expansion.Semantic proximity Read ↗

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