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Marshall syndrome
Relevant markers:
HypertelorismParents markers:EyesFacePalate
Involved genes:
(gene — definition — chromosome)1p22 — gène alpha-1 polypeptide du collagène XI (COL11A1) — 1 Inheritance mode: AD Other online databases: OrphaNet: ORPHA560, OMIM References: 2010 Pediatr Dermatology Case report Read on PubMed 2012 J Med Genet. Read on PubMed Login for more details.