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3. Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromata. Leppig KA; Kaplan P; Viskochil D; Weaver M; Ortenberg J; Stephens K Am J Med Genet; 1997 Dec; 73(2):197-204. PubMed ID: 9409873 [TBL] [Abstract][Full Text] [Related]
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8. High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions. Baumer A; Dutly F; Balmer D; Riegel M; Tükel T; Krajewska-Walasek M; Schinzel AA Hum Mol Genet; 1998 May; 7(5):887-94. PubMed ID: 9536094 [TBL] [Abstract][Full Text] [Related]
11. Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2. Trost D; Wiebe W; Uhlhaas S; Schwindt P; Schwanitz G J Med Genet; 2000 Jun; 37(6):452-4. PubMed ID: 10928854 [No Abstract] [Full Text] [Related]
12. The mechanisms involved in formation of deletions and duplications of 15q11-q13. Robinson WP; Dutly F; Nicholls RD; Bernasconi F; Peñaherrera M; Michaelis RC; Abeliovich D; Schinzel AA J Med Genet; 1998 Feb; 35(2):130-6. PubMed ID: 9580159 [TBL] [Abstract][Full Text] [Related]
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14. Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients. Kayes LM; Burke W; Riccardi VM; Bennett R; Ehrlich P; Rubenstein A; Stephens K Am J Hum Genet; 1994 Mar; 54(3):424-36. PubMed ID: 8116612 [TBL] [Abstract][Full Text] [Related]
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