^Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 725, 831. ISBN978-1-4160-2999-1.
^Allanson JE, Upadhyaya M, Watson GH, et al. (November 1991). "Watson syndrome: is it a subtype of type 1 neurofibromatosis?". J. Med. Genet. 28 (11): 752–6. doi:10.1136/jmg.28.11.752. PMC1017110. PMID 1770531.
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watson, syndrome, autosomal, dominant, condition, characterized, lisch, nodules, ocular, iris, axillary, inguinal, freckling, pulmonary, valvular, stenosis, relative, macrocephaly, short, stature, neurofibromas, allelic, same, gene, associated, with, neurofibr. Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris axillary inguinal freckling pulmonary valvular stenosis relative macrocephaly short stature and neurofibromas 1 Watson syndrome is allelic to NF1 the same gene associated with neurofibromatosis type 1 2 Watson syndromeSpecialtyMedical genetics See also EditWesterhof syndrome List of cutaneous conditionsReferences Edit Rapini Ronald P Bolognia Jean L Jorizzo Joseph L 2007 Dermatology 2 Volume Set St Louis Mosby pp 725 831 ISBN 978 1 4160 2999 1 Allanson JE Upadhyaya M Watson GH et al November 1991 Watson syndrome is it a subtype of type 1 neurofibromatosis J Med Genet 28 11 752 6 doi 10 1136 jmg 28 11 752 PMC 1017110 PMID 1770531 External links EditThis Genodermatoses article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Watson syndrome amp oldid 1050661633, wikipedia, wiki, book, books, library,
