165 related articles for article (PubMed ID: 3863482)
21. The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications.
Forster-Gibson CJ; Mulligan LM; Partington MW; Simpson NE; Holden JJ; White BN
J Neurogenet; 1985 Jun; 2(3):231-7. PubMed ID: 3860635
[TBL] [Abstract][Full Text] [Related]
22. [Familial mental retardation and the fragile X syndrome].
Veenema H; Pelckmans AJ; Geraedts JP; Van Leeuwen I; Zvelebil N
Tijdschr Kindergeneeskd; 1984 Feb; 52(1):9-15. PubMed ID: 6585033
[TBL] [Abstract][Full Text] [Related]
23. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
Vincent A; Dahl N; Oberlé I; Hanauer A; Mandel JL; Malmgren H; Pettersson U
Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
[TBL] [Abstract][Full Text] [Related]
24. Fragile X trait in a large kindred: transmission also through normal males.
Van Roy BC; De Smedt MC; Raes RA; Dumon JE; Leroy JG
J Med Genet; 1983 Aug; 20(4):286-9. PubMed ID: 6620329
[TBL] [Abstract][Full Text] [Related]
25. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
Arveiler B; Oberlé I; Vincent A; Hofker MH; Pearson PL; Mandel JL
Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
[TBL] [Abstract][Full Text] [Related]
26. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.
Sood R; Mulligan LM; Poon R; White BN; Holden JJ
Am J Hum Genet; 1990 Sep; 47(3):395-402. PubMed ID: 1975476
[TBL] [Abstract][Full Text] [Related]
27. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
[TBL] [Abstract][Full Text] [Related]
28. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
Brown WT; Gross AC; Chan CB; Jenkins EC
Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490
[TBL] [Abstract][Full Text] [Related]
29. Marker X-associated mental retardation. A study of 150 retarded males.
Kähkönen M; Leisti J; Wilska M; Varonen S
Clin Genet; 1983 Jun; 23(6):397-404. PubMed ID: 6576874
[TBL] [Abstract][Full Text] [Related]
30. Frequency of the fragile X syndrome in Japanese mentally retarded males.
Arinami T; Kondo I; Nakajima S
Hum Genet; 1986 Aug; 73(4):309-12. PubMed ID: 3744362
[TBL] [Abstract][Full Text] [Related]
31. Twelve families with fragile X(q27).
Webb T; Thake A; Todd J
J Med Genet; 1986 Oct; 23(5):400-6. PubMed ID: 3783616
[TBL] [Abstract][Full Text] [Related]
32. The strength of association between fragile (X) chromosome presence and mental retardation.
Silverman W; Lubin R; Jenkins EC; Brown WT
Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008
[TBL] [Abstract][Full Text] [Related]
33. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.
Mulligan LM; Phillips MA; Forster-Gibson CJ; Beckett J; Partington MW; Simpson NE; Holden JJ; White BN
Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332
[TBL] [Abstract][Full Text] [Related]
34. Martin-Bell syndrome fra(X) (q28) in a Sri Lankan family.
Soysa P; Senanayahe M; Mikkelsen M; Poulsen H
J Ment Defic Res; 1982 Dec; 26 (Pt 4)():251-7. PubMed ID: 7169632
[TBL] [Abstract][Full Text] [Related]
35. Klinefelter syndrome and associated fragile-X syndrome.
Pueschel SM; O'Brien MM; Padre-Mendoza T
J Ment Defic Res; 1987 Mar; 31 ( Pt 1)():73-9. PubMed ID: 3585988
[TBL] [Abstract][Full Text] [Related]
36. Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.
Giannelli F; Morris AH; Garrett C; Daker M; Thurston C; Smith CA
Ann Hum Genet; 1987 May; 51(2):107-24. PubMed ID: 3674751
[TBL] [Abstract][Full Text] [Related]
37. Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.
Buchanan JA; Buckton KE; Gosden CM; Newton MS; Clayton JF; Christie S; Hastie N
Hum Genet; 1987 Jun; 76(2):165-72. PubMed ID: 3038730
[TBL] [Abstract][Full Text] [Related]
38. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
Fishburn J; Turner G; Daniel A; Brookwell R
Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625
[TBL] [Abstract][Full Text] [Related]
39. Fragile X syndrome: a unique mutation in man.
Nussbaum RL; Ledbetter DH
Annu Rev Genet; 1986; 20():109-45. PubMed ID: 3545058
[No Abstract] [Full Text] [Related]
40. Genetic linkage heterogeneity in the fragile X syndrome.
Brown WT; Gross AC; Chan CB; Jenkins EC
Hum Genet; 1985; 71(1):11-8. PubMed ID: 2993154
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
