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Article

Interstitial 10p11.23-p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism.

American journal of medical genetics. Part A - 1 Oct 2014

Mroczkowski Henry J, Arnold Georgianne, Schneck Francis X, Rajkovic Aleksandar, Yatsenko Svetlana A

Abstract excerpt

Cryptorchidism is the most common genital problem encountered in males and is associated with many chromosomal disorders; however, the genetic factors are mostly unknown. To delineate critical genes affecting testicular migration, we performed genotype-phenotype correlation in patients with deletions involving the proximal short arm of chromosome 10 (10p11-p12), a rare abnormality characterized by developmental...

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Share to Chromosome Deletion
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 10

Share to Craniofacial Abnormalities

Share to Cryptorchidism

Share to Developmental Disabilities

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Source

Identifiers

PMID: 25073539
DOI: 10.1002/ajmg.a.36627

Genes

MKX
MPP7
SOX9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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