184 related articles for article (PubMed ID: 2543076)
21. Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia.
Pulst SM; Pribyl T; Barker DF; Riccardi VM; Ren M; Yaari H; Korenberg JR
Am J Med Genet; 1991 Jul; 40(1):84-7. PubMed ID: 1909491
[TBL] [Abstract][Full Text] [Related]
22. Progress towards the isolation and characterization of the genes causing neurofibromatosis.
Menon AG; Gusella JF; Seizinger BR
Cancer Surv; 1990; 9(4):689-702. PubMed ID: 2129297
[TBL] [Abstract][Full Text] [Related]
23. Refined physical and genetic mapping of the NF1 region on chromosome 17.
Fain PR; Goldgar DE; Wallace MR; Collins FS; Wright E; Nguyen K; Barker DF
Am J Hum Genet; 1989 Nov; 45(5):721-8. PubMed ID: 2573276
[TBL] [Abstract][Full Text] [Related]
24. Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 families.
Stephens K; Riccardi VM; Rising M; Ng S; Green P; Collins FS; Rediker KS; Powers JA; Parker C; Donis-Keller H
Genomics; 1987 Dec; 1(4):353-7. PubMed ID: 2896629
[TBL] [Abstract][Full Text] [Related]
25. Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.
Hsiao MC; Piotrowski A; Alexander J; Callens T; Fu C; Mikhail FM; Claes KB; Messiaen L
Hum Mutat; 2014 Jul; 35(7):891-8. PubMed ID: 24760680
[TBL] [Abstract][Full Text] [Related]
26. Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.
Kittur SD; Bagdon MM; Lubs ML; Phillips JA; Murray JC; Slaugenhaupt SA; Chakravarti A; Adler WH
Am J Hum Genet; 1989 Jan; 44(1):48-50. PubMed ID: 2491782
[TBL] [Abstract][Full Text] [Related]
27. The gene for von Recklinghausen neurofibromatosis (NF1) maps to the pericentromeric region of chromosome 17 in Chinese families.
Xu WM; Cheng XF; Hong LS; Liu LZ; Bao Y; He RG; Zhou XJ; Shen ZZ; Qui WQ; Ponder B
Genomics; 1991 Aug; 10(4):1090-2. PubMed ID: 1916815
[TBL] [Abstract][Full Text] [Related]
28. Familial reciprocal translocation t(17;19) (q11.2;q13.2) associated with neurofibromatosis type 1, including one patient with non-Hodgkin lymphoma and an additional t(14;20) in B lymphocytes.
Fahsold R; Habash T; Trautmann U; Haustein A; Pfeiffer RA
Hum Genet; 1995 Jul; 96(1):65-9. PubMed ID: 7607657
[TBL] [Abstract][Full Text] [Related]
29. Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17.
Diehl SR; Boehnke M; Erickson RP; Baxter AB; Bruce MA; Lieberman JL; Platt DJ; Ploughman LM; Seiler KA; Sweet AM
Genomics; 1987 Dec; 1(4):361-3. PubMed ID: 2896631
[TBL] [Abstract][Full Text] [Related]
30. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
[TBL] [Abstract][Full Text] [Related]
31. The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions.
Kehrer-Sawatzki H; Häussler J; Krone W; Bode H; Jenne DE; Mehnert KU; Tümmers U; Assum G
Hum Genet; 1997 Feb; 99(2):237-47. PubMed ID: 9048928
[TBL] [Abstract][Full Text] [Related]
32. 17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one.
Asamoah A; North K; Doran S; Wagstaff J; Ogle R; Collins FS; Korf BR
Am J Med Genet; 1995 Aug; 60(4):312-6. PubMed ID: 7485267
[TBL] [Abstract][Full Text] [Related]
33. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F
Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
[TBL] [Abstract][Full Text] [Related]
34. Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.
Menon AG; Anderson KM; Riccardi VM; Chung RY; Whaley JM; Yandell DW; Farmer GE; Freiman RN; Lee JK; Li FP
Proc Natl Acad Sci U S A; 1990 Jul; 87(14):5435-9. PubMed ID: 2142531
[TBL] [Abstract][Full Text] [Related]
35. Detailed mapping around the breakpoint of (3;8) translocation in familial renal cell carcinoma and FRA3B.
Yamakawa K; Takahashi E; Murata M; Okui K; Yokoyama S; Nakamura Y
Genomics; 1992 Oct; 14(2):412-6. PubMed ID: 1427857
[TBL] [Abstract][Full Text] [Related]
36. Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.
Seizinger BR; Rouleau GA; Lane AH; Farmer G; Ozelius LJ; Haines JL; Parry DM; Korf BR; Pericak-Vance MA; Faryniarz AG
Genomics; 1987 Dec; 1(4):346-8. PubMed ID: 2896628
[TBL] [Abstract][Full Text] [Related]
37. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
Laureys GG
Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.
Van Roy N; Laureys G; Van Gele M; Opdenakker G; Miura R; van der Drift P; Chan A; Versteeg R; Speleman F
Eur J Cancer; 1997 Oct; 33(12):1974-8. PubMed ID: 9516836
[TBL] [Abstract][Full Text] [Related]
40. An EcoRI RFLP in the 5' region of the human NF1 gene.
Reyniers E; De Boulle K; Marchuk DA; Andersen LB; Collins FS; Willems PJ
Hum Genet; 1993 Dec; 92(6):631. PubMed ID: 7903272
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
