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searching for Mirhosseini–Holmes–Walton syndrome 2 found (3 total)

alternate case: mirhosseini–Holmes–Walton syndrome

Microcephaly lymphoedema chorioretinal dysplasia (377 words) [view diff] exact match in snippet view article find links to article

as autosomal dominant, autosomal recessive (MIM 251270 or Mirhosseini-Holmes-Walton syndrome) or X-linked trait. The distinct facial feature include upslanting
Cohen syndrome (359 words) [view diff] exact match in snippet view article find links to article
evidence that this syndrome has the same genetic cause as Mirhosseini-Holmes-Walton syndrome. Cohen syndrome is diagnosed by clinical examination, but