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2. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage. Charrow J; Listernick R; Ward K Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833 [TBL] [Abstract][Full Text] [Related]
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4. Manifestations of the tongue in Neurofibromatosis type 1. Bongiorno MR; Pistone G; Aricò M Oral Dis; 2006 Mar; 12(2):125-9. PubMed ID: 16476032 [TBL] [Abstract][Full Text] [Related]
5. Familial café au lait spots: a variant of neurofibromatosis type 1. Abeliovich D; Gelman-Kohan Z; Silverstein S; Lerer I; Chemke J; Merin S; Zlotogora J J Med Genet; 1995 Dec; 32(12):985-6. PubMed ID: 8825931 [TBL] [Abstract][Full Text] [Related]
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9. Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus. Ahlbom BE; Dahl N; Zetterqvist P; Annerén G Clin Genet; 1995 Aug; 48(2):85-9. PubMed ID: 7586657 [TBL] [Abstract][Full Text] [Related]
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14. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Brems H; Chmara M; Sahbatou M; Denayer E; Taniguchi K; Kato R; Somers R; Messiaen L; De Schepper S; Fryns JP; Cools J; Marynen P; Thomas G; Yoshimura A; Legius E Nat Genet; 2007 Sep; 39(9):1120-6. PubMed ID: 17704776 [TBL] [Abstract][Full Text] [Related]
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17. Head and neck manifestations of neurofibromatosis. White AK; Smith RJ; Bigler CR; Brooke WF; Schauer PR Laryngoscope; 1986 Jul; 96(7):732-7. PubMed ID: 3088347 [TBL] [Abstract][Full Text] [Related]
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20. A family with coexistent von Recklinghausen's neurofibromatosis and von Hippel-Lindau's disease. Diseases possibly derived from a common gene. Tishler PV Neurology; 1975 Sep; 25(9):840-4. PubMed ID: 808759 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]