Watson syndrome: is it a subtype of type 1 neurofibromatosis?

Over 20 years ago, Watson described three families with a condition characterised by pulmonary valvular stenosis, café au lait patches, and dull intelligence. Short stature is an additional feature of this autosomal dominant condition. A fourth family with Watson syndrome has since been reported. We...

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Vydáno v:J Med Genet
Hlavní autoři: Allanson, J E, Upadhyaya, M, Watson, G H, Partington, M, MacKenzie, A, Lahey, D, MacLeod, H, Sarfarazi, M, Broadhead, W, Harper, P S
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 1991
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017110/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1770531/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.11.752
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