160 related articles for article (PubMed ID: 2018068)
1. Fragile X screening program in New York State.
Nolin SL; Snider DA; Jenkins EC; Brown WT; Krawczun M; Stetka D; Houck G; Dobkin CS; Strong G; Smith-Dobransky G
Am J Med Genet; 1991; 38(2-3):251-5. PubMed ID: 2018068
[TBL] [Abstract][Full Text] [Related]
2. New York State screening program for fragile X syndrome: a progress report.
Nolin SL; Snider DA; Jenkins EC; Dobkin CS; Patchell K; Krawczun M; Strong G; Colwell M; Victor A; Payyapilli T
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):328-32. PubMed ID: 1605206
[TBL] [Abstract][Full Text] [Related]
3. Fragile X screening program in a Spanish region.
Gabarrón J; Lopez I; Glover G; Carbonell P
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):333-8. PubMed ID: 1605207
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Institutional screening for the fragile X syndrome.
Hagerman R; Berry R; Jackson AW; Campbell J; Smith AC; McGavran L
Am J Dis Child; 1988 Nov; 142(11):1216-21. PubMed ID: 3177330
[TBL] [Abstract][Full Text] [Related]
6. Cytogenetic diagnosis of the fragile X syndrome: efficiency, utilization, and trends.
Shapiro LR; Wilmot PL; Shapiro DA; Pettersen IM; Casamassima AC
Am J Med Genet; 1991; 38(2-3):408-10. PubMed ID: 2018082
[TBL] [Abstract][Full Text] [Related]
7. A 15-item checklist for screening mentally retarded males for the fragile X syndrome.
Butler MG; Mangrum T; Gupta R; Singh DN
Clin Genet; 1991 May; 39(5):347-54. PubMed ID: 1860251
[TBL] [Abstract][Full Text] [Related]
8. Fragile site X chromosomes in mentally retarded boys.
Moon HR; Moon SY
J Korean Med Sci; 1993 Jun; 8(3):192-6. PubMed ID: 8240748
[TBL] [Abstract][Full Text] [Related]
9. Fragile X checklist.
Hagerman RJ; Amiri K; Cronister A
Am J Med Genet; 1991; 38(2-3):283-7. PubMed ID: 2018072
[TBL] [Abstract][Full Text] [Related]
10. Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.
Arinami T; Kondo I; Nakajima S; Hamaguchi H
Hum Genet; 1987 Aug; 76(4):344-7. PubMed ID: 3610153
[TBL] [Abstract][Full Text] [Related]
11. Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.
Butler MG; Singh DN
J Intellect Disabil Res; 1993 Apr; 37 ( Pt 2)(Pt 2):131-42. PubMed ID: 8481611
[TBL] [Abstract][Full Text] [Related]
12. Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives.
Sutherland GR
Hum Genet; 1979; 53(1):23-7. PubMed ID: 535898
[TBL] [Abstract][Full Text] [Related]
13. Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28).
Nielsen KB; Tommerup N; Dyggve HV; Schou C
Hum Genet; 1982; 61(2):113-7. PubMed ID: 6215327
[TBL] [Abstract][Full Text] [Related]
14. Fragile X mental retardation: prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern.
Sanfilippo S; Ragusa RM; Musumeci S; Neri G
Am J Med Genet; 1986; 23(1-2):589-95. PubMed ID: 3953669
[TBL] [Abstract][Full Text] [Related]
15. The Martin-Bell syndrome in South Africa.
Venter PA; Op't Hof J; Coetzee DJ
Am J Med Genet; 1986; 23(1-2):597-610. PubMed ID: 3953670
[TBL] [Abstract][Full Text] [Related]
16. A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
Haspeslagh M; Fryns JP; Holvoet M; Collen G; Dierck G; Baeke J; van den Berghe H
Clin Genet; 1991 Jun; 39(6):434-41. PubMed ID: 1863991
[TBL] [Abstract][Full Text] [Related]
17. Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico.
González-del Angel A; Vidal S; Saldaña Y; del Castillo V; Angel Alcántara M; Macías M; Pedro Luna J; Orozco L
Ann Genet; 2000; 43(1):29-34. PubMed ID: 10818218
[TBL] [Abstract][Full Text] [Related]
18. Fragile-X mutation and Klinefelter syndrome: a reappraisal.
Filippi G; Pecile V; Rinaldi A; Siniscalco M
Am J Med Genet; 1988; 30(1-2):99-107. PubMed ID: 3177482
[TBL] [Abstract][Full Text] [Related]
19. Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study Group.
de Vries BB; Mohkamsing S; van den Ouweland AM; Mol E; Gelsema K; van Rijn M; Tibben A; Halley DJ; Duivenvoorden HJ; Oostra BA; Niermeijer MF
J Med Genet; 1999 Jun; 36(6):467-70. PubMed ID: 10874635
[TBL] [Abstract][Full Text] [Related]
20. Applicability of a checklist for clinical screening of the fragile X syndrome.
Arvio M; Peippo M; Simola KO
Clin Genet; 1997 Oct; 52(4):211-5. PubMed ID: 9383025
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]