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Article

VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.

American journal of medical genetics - 1 Jan 1994

Corsello G, Giuffrè L

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 8172244
DOI: 10.1002/ajmg.1320490133

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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.

Related research

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VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.PMID 8172244Read ↗

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VACTERL with hydrocephalus: Family with X-linked VACTERL-HSemantic proximity Read ↗

Evidence for inheritance in patients with VACTERL associationSemantic proximity Read ↗

X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.Semantic proximity Read ↗

[From gene to disease; X-linked hydrocephalus and LiCAM].Semantic proximity Read ↗

A case of complete form of pachydermoperiostosis with SLCO2A1 mutations.Semantic proximity Read ↗

Sporadic neonatal Fanconi's anemia with VACTERL association.Semantic proximity Read ↗

Sporadic VACTERL association in a Japanese family with Sjögren-Larsson syndrome.Semantic proximity Read ↗

Recurrent congenital hydrocephalus: two case reports and counseling highlights.Semantic proximity Read ↗

X-linked hydrocephalus: another two families with an L1 mutation.Semantic proximity Read ↗

VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal community.Semantic proximity Read ↗

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