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.
141 related articles for article (PubMed ID: 2902795)
21. Molecular diagnosis of the fragile X [Fra (X)] syndrome: calculation of risks based on flanking DNA markers in small phase-unknown families. Bridge PJ; Lillicrap DP Am J Med Genet; 1989 May; 33(1):92-9. PubMed ID: 2568753 [TBL] [Abstract][Full Text] [Related]
22. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation. Voelckel MA; Philip N; Piquet C; Pellissier MC; Oberlé I; Birg F; Mattei MG; Mattei JF Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838 [TBL] [Abstract][Full Text] [Related]
23. RN1, a new polymorphic marker near the fragile X locus. (HGM10 assignment DXS 369). Hupkes PE; van Bennekom CA; van Oost BA; Oostra BA Nucleic Acids Res; 1990 Feb; 18(3):692. PubMed ID: 1968631 [No Abstract] [Full Text] [Related]
24. An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis. Forster-Gibson CJ; Mulligan LM; Simpson NE; White BN; Holden JJ Am J Med Genet; 1986; 23(1-2):665-83. PubMed ID: 3006491 [TBL] [Abstract][Full Text] [Related]
25. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304. Dahl N; Malmgren H; Pettersson U; Holmgren G; Seemanová E; Gustavson KH Am J Med Genet; 1991; 38(2-3):319-21. PubMed ID: 1673304 [TBL] [Abstract][Full Text] [Related]
26. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304. Goonewardena P; Brown WT; Gross AC; Ferrando C; Dobkin C; Romano V; Bosco P; Ceratto N; Pettersson U; Dahl N Am J Med Genet; 1991; 38(2-3):322-7. PubMed ID: 1673305 [TBL] [Abstract][Full Text] [Related]
27. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8. Brown WT; Gross AC; Goonewardena P; Ferrando C; Dobkin C; Jenkins EC Am J Med Genet; 1991; 38(2-3):343-6. PubMed ID: 1673308 [TBL] [Abstract][Full Text] [Related]
28. Multilocus analysis of the fragile X syndrome. Brown WT; Gross A; Chan C; Jenkins EC; Mandel JL; Oberlé I; Arveiler B; Novelli G; Thibodeau S; Hagerman R Hum Genet; 1988 Mar; 78(3):201-5. PubMed ID: 3162224 [TBL] [Abstract][Full Text] [Related]
29. Multipoint linkage analysis of DXS369 and DXS304 in fragile X families. van Oost BA; Smits A; Dreesen JC; Smeets D; Perdon L; van Bennekom CA; Dahl N; Bakker E; Oostra BA Am J Med Genet; 1991; 38(2-3):328-31. PubMed ID: 2018075 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. A new DNA marker tightly linked to the fragile X locus (FRAXA). Suthers GK; Callen DF; Hyland VJ; Kozman HM; Baker E; Eyre H; Harper PS; Roberts SH; Hors-Cayla MC; Davies KE Science; 1989 Dec; 246(4935):1298-300. PubMed ID: 2573953 [TBL] [Abstract][Full Text] [Related]
32. Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes. Goonewardena P; Gustavson KH; Holmgren G; Tolun A; Chotai J; Johnsen E; Pettersson U Clin Genet; 1986 Oct; 30(4):249-54. PubMed ID: 2878749 [TBL] [Abstract][Full Text] [Related]
33. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3. Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524 [TBL] [Abstract][Full Text] [Related]
34. Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome. Patterson MN; Bell MV; Bloomfield J; Flint T; Dorkins H; Thibodeau SN; Schaid D; Bren G; Schwartz CE; Wieringa B Genomics; 1989 May; 4(4):570-8. PubMed ID: 2744766 [TBL] [Abstract][Full Text] [Related]
35. Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family. Anvret M; Gillberg C; Wahlström J; Albertsson-Wikland K; Davies K Clin Genet; 1988 Oct; 34(4):265-71. PubMed ID: 2906823 [TBL] [Abstract][Full Text] [Related]
36. Linkage and risk assessment in fragile X families using new DNA probes at Xq27. Carpenter NJ; Swartz-Boyd J; Prichard JK; Lam T Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):312-9. PubMed ID: 1351365 [TBL] [Abstract][Full Text] [Related]
37. Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome. Dahl N; Hammarström-Heeroma K; Goonewardena P; Wadelius C; Gustavson KH; Holmgren G; van Ommen GJ; Pettersson U Hum Genet; 1989 Jun; 82(3):216-8. PubMed ID: 2567272 [TBL] [Abstract][Full Text] [Related]
38. New distal marker closely linked to the fragile X locus. Hulsebos TJ; Oostra BA; Broersen S; Smits A; van Oost BA; Westerveld A Hum Genet; 1991 Jul; 87(3):369-72. PubMed ID: 1677926 [TBL] [Abstract][Full Text] [Related]
39. A new DNA probe proximal to and closely linked to fragile X. Carpenter NJ; Veenema H; Bakker E; Hofker MH; Pearson PL Am J Med Genet; 1987 Jul; 27(3):731-2. PubMed ID: 2888310 [No Abstract] [Full Text] [Related]
40. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]