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2. 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]
3. The fragile X syndrome. Brown WT Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518 [TBL] [Abstract][Full Text] [Related]
4. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation. Rousseau F; Heitz D; Biancalana V; Blumenfeld S; Kretz C; Boué J; Tommerup N; Van Der Hagen C; DeLozier-Blanchet C; Croquette MF N Engl J Med; 1991 Dec; 325(24):1673-81. PubMed ID: 1944467 [TBL] [Abstract][Full Text] [Related]
5. Fragile X mental retardation syndrome: DNA diagnosis and carrier detection in New Zealand families. Neville L; Cochrane J; Fitzgerald P; Kennedy M N Z Med J; 1995 Oct; 108(1009):404-6. PubMed ID: 7478333 [TBL] [Abstract][Full Text] [Related]
6. [The diagnosis of mental retardation in fragile X syndrome is revolutionized by molecular genetics]. Lemire M; Rousseau F Union Med Can; 1993; 122(1):23-9. PubMed ID: 8465472 [TBL] [Abstract][Full Text] [Related]
8. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14. Mulley JC; Gedeon AK; Thorn KA; Bates LJ; Sutherland GR Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Fragile-X syndrome in east Finland: molecular approach to genetic and prenatal diagnosis. Ryynänen M; Pulkkinen L; Kirkinen P; Saarikoski S Am J Med Genet; 1994 Jul; 51(4):463-5. PubMed ID: 7943020 [TBL] [Abstract][Full Text] [Related]
11. Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis. Vincent A; Heitz D; Petit C; Kretz C; Oberlé I; Mandel JL Nature; 1991 Feb; 349(6310):624-6. PubMed ID: 1672039 [TBL] [Abstract][Full Text] [Related]
12. Fragile X-linked mental retardation and the difficulties of reverse genetics. Jordan BR Bioessays; 1991 May; 13(5):243-51. PubMed ID: 1679986 [TBL] [Abstract][Full Text] [Related]
13. [Mental retardation linked to fragility of chromosome X: current knowledge]. Mattei JF; Mattei MG; Auger M; Giraud F J Genet Hum; 1984 Jul; 32(3):167-92. PubMed ID: 6237176 [TBL] [Abstract][Full Text] [Related]
14. Genetics and expression of the fragile X syndrome. Brown WT; Jenkins EC; Gross AC; Chan CB; Wisniewski K; Cohen IL; Miezejeski CM Ups J Med Sci Suppl; 1987; 44():137-54. PubMed ID: 2895523 [TBL] [Abstract][Full Text] [Related]
15. A new DNA probe of potential use for diagnosis of the fragile-X syndrome. Lucotte G Ann Genet; 1990; 33(2):109-10. PubMed ID: 1978629 [TBL] [Abstract][Full Text] [Related]
16. [DNA diagnosis of fragile X syndrome in a family. A new type of heredity--dynamic mutations]. Eiken HG; Boman H; Apold J Tidsskr Nor Laegeforen; 1993 Oct; 113(26):3236-9. PubMed ID: 8236216 [TBL] [Abstract][Full Text] [Related]
17. Fragile X syndrome. Laxova R Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis and carrier screening for fragile X by PCR. Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Stark-Houck S; Brophy P; Duncan C; Dobkin C; Jenkins E Am J Med Genet; 1996 Jul; 64(1):191-5. PubMed ID: 8826474 [TBL] [Abstract][Full Text] [Related]
19. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation. Pembrey ME; Winter RM; Davies KE Am J Med Genet; 1985 Aug; 21(4):709-17. PubMed ID: 4040705 [TBL] [Abstract][Full Text] [Related]
20. [The molecular genetics of the fragile X syndrome. Its molecular diagnosis by DNA probes]. Giné R; Espinás ML; Antich J; Carballo M Med Clin (Barc); 1992 Feb; 98(4):121-4. PubMed ID: 1552760 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]