These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
165 related articles for article (PubMed ID: 9598729)
1. Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome. van Asperen CJ; Overweg-Plandsoen WC; Cnossen MH; van Tijn DA; Hennekam RC J Med Genet; 1998 Apr; 35(4):323-7. PubMed ID: 9598729 [TBL] [Abstract][Full Text] [Related]
2. Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2. Streubel B; Latta E; Kehrer-Sawatzki H; Hoffmann GF; Fonatsch C; Rehder H Am J Med Genet; 1999 Nov; 87(1):12-6. PubMed ID: 10528240 [TBL] [Abstract][Full Text] [Related]
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]
4. Spectrum of NSD1 mutations in Sotos and Weaver syndromes. Rio M; Clech L; Amiel J; Faivre L; Lyonnet S; Le Merrer M; Odent S; Lacombe D; Edery P; Brauner R; Raoul O; Gosset P; Prieur M; Vekemans M; Munnich A; Colleaux L; Cormier-Daire V J Med Genet; 2003 Jun; 40(6):436-40. PubMed ID: 12807965 [TBL] [Abstract][Full Text] [Related]
5. Extensively high load of internal tumors determined by whole body MRI scanning in a patient with neurofibromatosis type 1 and a non-LCR-mediated 2-Mb deletion in 17q11.2. Kehrer-Sawatzki H; Kluwe L; Fünsterer C; Mautner VF Hum Genet; 2005 May; 116(6):466-75. PubMed ID: 15776250 [TBL] [Abstract][Full Text] [Related]
6. Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism. Kayes LM; Riccardi VM; Burke W; Bennett RL; Stephens K J Med Genet; 1992 Oct; 29(10):686-90. PubMed ID: 1359144 [TBL] [Abstract][Full Text] [Related]
8. Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth. Ferrari L; Scuvera G; Tucci A; Bianchessi D; Rusconi F; Menni F; Battaglioli E; Milani D; Riva P Hum Genet; 2017 Oct; 136(10):1329-1339. PubMed ID: 28776093 [TBL] [Abstract][Full Text] [Related]
9. Extended runs of homozygosity at 17q11.2: an association with type-2 NF1 deletions? Roehl AC; Cooper DN; Kluwe L; Helbrich A; Wimmer K; Högel J; Mautner VF; Kehrer-Sawatzki H Hum Mutat; 2010 Mar; 31(3):325-34. PubMed ID: 20052761 [TBL] [Abstract][Full Text] [Related]
10. Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis. Bartsch O; Vlcková Z; Erdogan F; Ullmann R; Novotná D; Spiegel M; Beyer V; Haaf T; Zechner U; Seemanová E Cytogenet Genome Res; 2007; 119(1-2):158-64. PubMed ID: 18160797 [TBL] [Abstract][Full Text] [Related]
11. A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features. Oktenli C; Saglam M; Demirbas S; Thompson P; Upadhyaya M; Consoli C; Ulucan H; Koz C; Durukan AH; Bozkurt A; Koc B; Kocar IH; Gul D Clin Dysmorphol; 2003 Jul; 12(3):199-201. PubMed ID: 14564162 [TBL] [Abstract][Full Text] [Related]
12. [Developmental manifestation in children with neurofibromatosis type 1]. Cohen R; Shuper A Harefuah; 2010 Jan; 149(1):49-52, 61. PubMed ID: 20422842 [TBL] [Abstract][Full Text] [Related]
13. A case of Miller-Dieker syndrome in a family with neurofibromatosis type I. King A; Upadhyaya M; Penney C; Doshi R Acta Neuropathol; 2000 Apr; 99(4):425-7. PubMed ID: 10787042 [TBL] [Abstract][Full Text] [Related]
14. Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome. Riva P; Castorina P; Manoukian S; Dalprà L; Doneda L; Marini G; den Dunnen J; Larizza L Hum Genet; 1996 Dec; 98(6):646-50. PubMed ID: 8931693 [TBL] [Abstract][Full Text] [Related]
15. Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions. Mautner VF; Kluwe L; Friedrich RE; Roehl AC; Bammert S; Högel J; Spöri H; Cooper DN; Kehrer-Sawatzki H J Med Genet; 2010 Sep; 47(9):623-30. PubMed ID: 20543202 [TBL] [Abstract][Full Text] [Related]
16. Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association. Bahuau M; Flintoff W; Assouline B; Lyonnet S; Le Merrer M; Prieur M; Guilloud-Bataille M; Feingold N; Munnich A; Vidaud M; Vidaud D Am J Med Genet; 1996 Dec; 66(3):347-55. PubMed ID: 8985499 [TBL] [Abstract][Full Text] [Related]
17. A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2. Bengesser K; Cooper DN; Steinmann K; Kluwe L; Chuzhanova NA; Wimmer K; Tatagiba M; Tinschert S; Mautner VF; Kehrer-Sawatzki H Hum Mutat; 2010 Jun; 31(6):742-51. PubMed ID: 20506354 [TBL] [Abstract][Full Text] [Related]
18. Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. Douglas J; Cilliers D; Coleman K; Tatton-Brown K; Barker K; Bernhard B; Burn J; Huson S; Josifova D; Lacombe D; Malik M; Mansour S; Reid E; Cormier-Daire V; Cole T; ; Rahman N Nat Genet; 2007 Aug; 39(8):963-5. PubMed ID: 17632510 [TBL] [Abstract][Full Text] [Related]
19. Do NF1 gene deletions result in a characteristic phenotype? Tonsgard JH; Yelavarthi KK; Cushner S; Short MP; Lindgren V Am J Med Genet; 1997 Nov; 73(1):80-6. PubMed ID: 9375928 [TBL] [Abstract][Full Text] [Related]
20. Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene. Gervasini C; Venturin M; Orzan F; Friso A; Clementi M; Tenconi R; Larizza L; Riva P Genomics; 2005 Feb; 85(2):273-9. PubMed ID: 15676286 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]