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Article

Genomics of human dysmorphogenesis.

American journal of medical genetics - 15 Jan 1992

Wilson G N

Abstract excerpt

A survey of Mendelian Inheritance in Man emphasizes the large Mendelian contribution to human dysmorphogenesis and contrasts single gene conditions with chromosomal disorders. There were 1761 conditions that involved altered morphogenesis (49% of disease entries), including 1040 multiple defect s...

Topics

Chromosome Aberrations
Chromosome Disorders
Chromosome Mapping
Congenital Abnormalities
Humans
Morphogenesis
Phenotype
Statistics as Topic
Syndrome

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1733168
DOI: 10.1002/ajmg.1320420211

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-1733168-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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