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

Next Steps in Prader-Willi Syndrome Research: On the Relationship between Genotype and Phenotype.

International journal of molecular sciences - 11 Oct 2022

Whittington Joyce, Holland Anthony

Abstract excerpt

This article reviews what we know of the phenotype and genotype of Prader-Willi syndrome and hypothesizes two possible paths from phenotype to genotype. It then suggests research that may strengthen the case for one or other of these hypotheses.

Read the complete abstract on PubMed

Topics

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

Share to Genotype
Share to Phenotype
Share to Prader-Willi Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 36292940
DOI: 10.3390/ijms232012089
PMCID: PMC9603642

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Next Steps in Prader-Willi Syndrome Research: On the Relationship between Genotype and Phenotype.PMID 36292940Read ↗

Neurobehavioral phenotype in Prader-Willi syndrome.Semantic proximity Read ↗

Relationship between phenotype and genotype of 102 Chinese newborns with Prader–Willi syndromeSemantic proximity Read ↗

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patientsSemantic proximity Read ↗

Relationship between clinical and genetic diagnosis of Prader-Willi syndrome.Semantic proximity Read ↗

The transition between the phenotypes of Prader-Willi syndrome during infancy and early childhood.Semantic proximity Read ↗

Genetics of childhood disorders: XV. Prader-Willi syndrome: genes, brain, and behavior.Semantic proximity Read ↗

Phenotype-karyotype-genotype correlations in Prader-Willi and Angelman syndromes: preliminary results.Semantic proximity Read ↗

Changing rates of genetic subtypes of Prader–Willi syndrome in the UKSemantic proximity Read ↗

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.Semantic proximity Read ↗

Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities.Semantic proximity Read ↗

The Spectrum of the Prader-Willi-like Pheno- and Genotype: A Review of the Literature.Semantic proximity Read ↗

The neonatal phenotype of Prader-Willi syndrome.Semantic proximity Read ↗

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