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

The syndrome of pachygyria, mental retardation, and arachnoid cysts maps to 11p15.

American journal of medical genetics. Part A - 1 Nov 2009

Bilguvar Kaya, Ozturk Ali K, Bayrakli Fatih, Guzel Aslan, DiLuna Michael L, Bayri Yasar, Tatli Mehmet, Tekes Selahaddin, Arlier Zulfikar, Yasuno Katsuhito, Mason Christopher E, Lifton Richard P, State Matthew W, Gunel Murat

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 Abnormalities, Multiple
Share to Blood Specimen Collection
Share to Chromosomes, Human, Pair 11

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Family

Share to Intellectual Disability

Share to Lissencephaly

Share to Lod Score

Source

Identifiers

PMID: 19876906
DOI: 10.1002/ajmg.a.33063

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

The syndrome of pachygyria, mental retardation, and arachnoid cysts maps to 11p15.PMID 19876906Read ↗

[Phenotypic and genetic characteristics of a child with 7p15 deletion syndrome].Semantic proximity Read ↗

Identification of 11p14.1-p15.3 deletion probably associated with short stature, relative macrocephaly, and delayed closure of the fontanelles.Semantic proximity Read ↗

Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionSemantic proximity Read ↗

Chromosome 15q11-q13 Duplication Syndrome: A Review of the Literature and 14 New Cases.Semantic proximity Read ↗

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

Advances in genetic mechanisms of hypothalamic dysfunction in Prader-Willi syndrome.Semantic proximity Read ↗

A novel 5p15.33-14.1 deletion and 4q34.24-35.2 duplication in a patient with mental retardation, dysmorphic features and severe speech delay.Semantic proximity Read ↗

Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability.Semantic proximity Read ↗

Genetic and Clinical Characteristics of Chromosome 15q11-q13 Duplication Syndrome in Chinese Children.Semantic proximity Read ↗

Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A.Semantic proximity Read ↗

Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an example.Semantic proximity Read ↗

A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature.Semantic proximity Read ↗

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