152 related articles for article (PubMed ID: 1605196)
1. Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype.
Dennis NR; Curtis G; Macpherson JN; Jacobs PA
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):232-6. PubMed ID: 1605196
[TBL] [Abstract][Full Text] [Related]
2. Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.
Oberlé I; Boué J; Croquette MF; Voelckel MA; Mattei MG; Mandel JL
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):224-31. PubMed ID: 1605195
[TBL] [Abstract][Full Text] [Related]
3. Fragile X syndrome.
Laxova R
Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.
Butler MG; Pratesi R; Vnencak-Jones CL
J Intellect Disabil Res; 1995 Dec; 39 ( Pt 6)(Pt 6):544-53. PubMed ID: 8746743
[TBL] [Abstract][Full Text] [Related]
6. Clinical, cytogenetic, and molecular analysis of three families with FRAXE.
Barnicoat AJ; Wang Q; Turk J; Green E; Mathew CG; Flynn G; Buckle V; Hirst M; Davies K; Bobrow M
J Med Genet; 1997 Jan; 34(1):13-7. PubMed ID: 9032643
[TBL] [Abstract][Full Text] [Related]
7. Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.
Hamel BC; Smits AP; de Graaff E; Smeets DF; Schoute F; Eussen BH; Knight SJ; Davies KE; Assman-Hulsmans CF; Oostra BA
Am J Hum Genet; 1994 Nov; 55(5):923-31. PubMed ID: 7977354
[TBL] [Abstract][Full Text] [Related]
8. The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
Proops R; Webb T
J Med Genet; 1981 Oct; 18(5):366-73. PubMed ID: 7328617
[TBL] [Abstract][Full Text] [Related]
9. Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.
Steinbach P
Hum Genet; 1986 Mar; 72(3):248-52. PubMed ID: 3957348
[TBL] [Abstract][Full Text] [Related]
10. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
Schinzel A; Largo RH
Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
Soudek D; Partington MW; Lawson JS
Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
[TBL] [Abstract][Full Text] [Related]
13. Mental status and fragile X expression in relation to FMR-1 gene mutation.
de Vries BB; Wiegers AM; de Graaff E; Verkerk AJ; Van Hemel JO; Halley DJ; Fryns JP; Curfs LM; Niermeijer MF; Oostra BA
Eur J Hum Genet; 1993; 1(1):72-9. PubMed ID: 8069653
[TBL] [Abstract][Full Text] [Related]
14. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
Rocchi M; Archidiacono N; Filippi G
J Genet Hum; 1987 Dec; 35(5):351-79. PubMed ID: 3437265
[TBL] [Abstract][Full Text] [Related]
15. The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
Hirst MC; Barnicoat A; Flynn G; Wang Q; Daker M; Buckle VJ; Davies KE; Bobrow M
Hum Mol Genet; 1993 Feb; 2(2):197-200. PubMed ID: 8499907
[TBL] [Abstract][Full Text] [Related]
16. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
Ventruto V; Stabile M; Gentile G; de Tollis G; Colantuoni M; Sirone P; Perone L; Lonardo F; Della Monica M; Fiore M
Ann Genet; 1986; 29(1):59-61. PubMed ID: 3487280
[TBL] [Abstract][Full Text] [Related]
17. Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.
Ramos FJ; Emanuel BS; Spinner NB
Am J Med Genet; 1992 Apr; 42(6):835-8. PubMed ID: 1532475
[TBL] [Abstract][Full Text] [Related]
18. Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.
Schmidt A
Hum Genet; 1982; 60(4):322-7. PubMed ID: 6955257
[TBL] [Abstract][Full Text] [Related]
19. Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.
Flynn GA; Hirst MC; Knight SJ; Macpherson JN; Barber JC; Flannery AV; Davies KE; Buckle VJ
J Med Genet; 1993 Feb; 30(2):97-100. PubMed ID: 8445629
[TBL] [Abstract][Full Text] [Related]
20. The fragile X syndrome.
de Vries BB; Halley DJ; Oostra BA; Niermeijer MF
J Med Genet; 1998 Jul; 35(7):579-89. PubMed ID: 9678703
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]