156 related articles for article (PubMed ID: 12447813)
1. [Prevention of fragile X syndrome by prenatal genetic diagnosis: advantages and controversial aspects].
Tejada MI
Rev Neurol; 2001 Oct; 33 Suppl 1():S14-9. PubMed ID: 12447813
[TBL] [Abstract][Full Text] [Related]
2. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
Mandel JL; Biancalana V
Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
[TBL] [Abstract][Full Text] [Related]
3. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
[TBL] [Abstract][Full Text] [Related]
4. [Diagnosis of fragile X syndrome].
Glover G; Bernabé MJ; Carbonell P
Rev Neurol; 2001 Oct; 33 Suppl 1():S6-9. PubMed ID: 12447811
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Timing of the absence of FMR1 expression in full mutation chorionic villi.
Willemsen R; Bontekoe CJ; Severijnen LA; Oostra BA
Hum Genet; 2002 Jun; 110(6):601-5. PubMed ID: 12107447
[TBL] [Abstract][Full Text] [Related]
7. Fragile X syndrome and fragile XE mental retardation.
Sutherland GR; Mulley JC
Prenat Diagn; 1996 Dec; 16(13):1199-211. PubMed ID: 9061751
[TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of 53 fragile X families with the probe StB12.3.
Puissant H; Malinge MC; Larget-Piet A; Martin D; Chauveau P; Odent S; Plessis G; Parent P; Lemarec B; Larget-Piet L
Am J Med Genet; 1994 Dec; 53(4):370-3. PubMed ID: 7864047
[TBL] [Abstract][Full Text] [Related]
9. [A genetic and molecular study of 85 families affected with the fragile X syndrome].
Milà Recasens M; Sánchez Díaz A; Glover López G; Castellví Bel S; Carbonell Meseguer P; Kruyer H; Ballesta Martínez F; Estivill Pallejà X
An Esp Pediatr; 1996 Mar; 44(3):250-6. PubMed ID: 8830601
[TBL] [Abstract][Full Text] [Related]
10. Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?
Reches A; Malcov M; Ben-Yosef D; Azem F; Amit A; Yaron Y
Prenat Diagn; 2009 Jan; 29(1):57-61. PubMed ID: 19097038
[TBL] [Abstract][Full Text] [Related]
11. Analysis of CGG variation through 642 meioses in Fragile X families.
Rifé M; Badenas C; Quintó L; Puigoriol E; Tazón B; Rodriguez-Revenga L; Jiménez L; Sánchez A; Milà M
Mol Hum Reprod; 2004 Oct; 10(10):773-6. PubMed ID: 15322225
[TBL] [Abstract][Full Text] [Related]
12. Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests.
Berkenstadt M; Ries-Levavi L; Cuckle H; Peleg L; Barkai G
Prenat Diagn; 2007 Nov; 27(11):991-4. PubMed ID: 17705235
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The frequency of fragile X syndrome among selected patients at Songklanagarind Hospital during 1991-1996, studied by cytogenetic and molecular methods.
Jinorose U; Vasiknanonte P; Limprasert P; Brown WT; Panich V
Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():69-74. PubMed ID: 9640603
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic tests for fragile X syndrome.
Oostra BA; Willemsen R
Expert Rev Mol Diagn; 2001 Jul; 1(2):226-32. PubMed ID: 11901818
[TBL] [Abstract][Full Text] [Related]
16. Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies.
Ryynänen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; Pertti K
Eur J Hum Genet; 1999; 7(2):212-6. PubMed ID: 10196705
[TBL] [Abstract][Full Text] [Related]
17. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
18. Molecular diagnosis of Fragile X syndrome.
Sofocleous C; Kolialexi A; Mavrou A
Expert Rev Mol Diagn; 2009 Jan; 9(1):23-30. PubMed ID: 19099346
[TBL] [Abstract][Full Text] [Related]
19. 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
Sofocleous C; Kitsiou S; Fryssira H; Kolialexi A; Kalaitzidaki M; Roma E; Tsangaris GT; Chistofidou C; Metaxotou C; Kanavakis E; Mavrou A
In Vivo; 2008; 22(4):451-5. PubMed ID: 18712171
[TBL] [Abstract][Full Text] [Related]
20. Molecular diagnosis and genetic counseling for fragile X mental retardation.
Pandey UB; Phadke SR; Mittal B
Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
