115 related articles for article (PubMed ID: 11313739)
1. XLMR genes: update 2000.
Chiurazzi P; Hamel BC; Neri G
Eur J Hum Genet; 2001 Feb; 9(2):71-81. PubMed ID: 11313739
[TBL] [Abstract][Full Text] [Related]
2. XLMR genes: update 1996.
Lubs HA; Chiurazzi P; Arena JF; Schwartz C; Tranebjaerg L; Neri G
Am J Med Genet; 1996 Jul; 64(1):147-57. PubMed ID: 8826465
[TBL] [Abstract][Full Text] [Related]
3. XLMR genes: update 1998.
Lubs H; Chiurazzi P; Arena J; Schwartz C; Tranebjaerg L; Neri G
Am J Med Genet; 1999 Apr; 83(4):237-47. PubMed ID: 10208155
[TBL] [Abstract][Full Text] [Related]
4. Splitting and lumping in the nosology of XLMR.
Stevenson RE
Am J Med Genet; 2000; 97(3):174-82. PubMed ID: 11449485
[TBL] [Abstract][Full Text] [Related]
5. [X-linked mental retardation--treatment scheme].
Lisik MZ; Sieroń AL
Wiad Lek; 2008; 61(4-6):146-53. PubMed ID: 18939366
[TBL] [Abstract][Full Text] [Related]
6. Towards identification of X-linked mental retardation genes: a proposal.
Mandel JL
Am J Med Genet; 1994 Jul; 51(4):550-2. PubMed ID: 7524320
[TBL] [Abstract][Full Text] [Related]
7. XLMR genes: update 1994.
Neri G; Chiurazzi P; Arena JF; Lubs HA
Am J Med Genet; 1994 Jul; 51(4):542-9. PubMed ID: 7943038
[TBL] [Abstract][Full Text] [Related]
8. Monogenic causes of X-linked mental retardation.
Chelly J; Mandel JL
Nat Rev Genet; 2001 Sep; 2(9):669-80. PubMed ID: 11533716
[TBL] [Abstract][Full Text] [Related]
9. Study of X-linked mental retardation (XLMR): summary of 61 families in the Miami/Greenwood Study.
Lubs HA; Schwartz CE; Stevenson RE; Arena JF
Am J Med Genet; 1996 Jul; 64(1):169-75. PubMed ID: 8826469
[TBL] [Abstract][Full Text] [Related]
10. Sixty years of X-linked mental retardation: a historical footnote.
Neri G; Opitz JM
Am J Med Genet; 2000; 97(3):228-33. PubMed ID: 11449492
[TBL] [Abstract][Full Text] [Related]
11. X-linked mental retardation (XLMR): from clinical conditions to cloned genes.
Chiurazzi P; Tabolacci E; Neri G
Crit Rev Clin Lab Sci; 2004; 41(2):117-58. PubMed ID: 15270552
[TBL] [Abstract][Full Text] [Related]
12. X-linked mental retardation and neurological symptoms: a nosological approach.
Schrander-Stumpel CT; Höweler CJ; Fryns JP
Genet Couns; 1995; 6(1):21-32. PubMed ID: 7794558
[TBL] [Abstract][Full Text] [Related]
13. X-linked mental retardation.
Lisik MZ; Sieron AL
Med Sci Monit; 2008 Nov; 14(11):RA221-9. PubMed ID: 18971887
[TBL] [Abstract][Full Text] [Related]
14. X-linked mental retardation: many genes for a complex disorder.
Ropers HH
Curr Opin Genet Dev; 2006 Jun; 16(3):260-9. PubMed ID: 16647850
[TBL] [Abstract][Full Text] [Related]
15. Detection and validation of copy number variation in X-linked mental retardation.
Bauters M; Weuts A; Vandewalle J; Nevelsteen J; Marynen P; Van Esch H; Froyen G
Cytogenet Genome Res; 2008; 123(1-4):44-53. PubMed ID: 19287138
[TBL] [Abstract][Full Text] [Related]
16. Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium.
de Brouwer AP; Yntema HG; Kleefstra T; Lugtenberg D; Oudakker AR; de Vries BB; van Bokhoven H; Van Esch H; Frints SG; Froyen G; Fryns JP; Raynaud M; Moizard MP; Ronce N; Bensalem A; Moraine C; Poirier K; Castelnau L; Saillour Y; Bienvenu T; Beldjord C; des Portes V; Chelly J; Turner G; Fullston T; Gecz J; Kuss AW; Tzschach A; Jensen LR; Lenzner S; Kalscheuer VM; Ropers HH; Hamel BC
Hum Mutat; 2007 Feb; 28(2):207-8. PubMed ID: 17221867
[TBL] [Abstract][Full Text] [Related]
17. Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three families.
Raynaud M; Moizard MP; Dessay B; Briault S; Toutain A; Gendrot C; Ronce N; Moraine C
Eur J Hum Genet; 2000 Apr; 8(4):253-8. PubMed ID: 10854107
[TBL] [Abstract][Full Text] [Related]
18. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
19. [Genetics of mental retardation].
Prieto García F
Neurologia; 1998 May; 13(5):218-22. PubMed ID: 9646628
[TBL] [Abstract][Full Text] [Related]
20. X-linked mental retardation: further lumping, splitting and emerging phenotypes.
Kleefstra T; Hamel BC
Clin Genet; 2005 Jun; 67(6):451-67. PubMed ID: 15857409
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
