Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 215

1.

Splitting and lumping in the nosology of XLMR.

Stevenson RE.

Am J Med Genet. 2000 Fall;97(3):174-82. Review.

PMID:
11449485
2.

XLMR genes: update 1992.

Neri G, Chiurazzi P, Arena F, Lubs HA, Glass IA.

Am J Med Genet. 1992 Apr 15-May 1;43(1-2):373-82. Review.

PMID:
1605215
3.

A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.

Shashi V, Berry MN, Shoaf S, Sciote JJ, Goldstein D, Hart TC.

Am J Hum Genet. 2000 Feb;66(2):469-79. Erratum in: Am J Hum Genet 2000 Apr;66(4):1472.

4.

[Update on the genetics of X-linked mental retardation].

Bahi-Buisson N, Chelly J, des Portes V.

Rev Neurol (Paris). 2006 Oct;162(10):952-63. Review. French.

PMID:
17028563
5.

XLMR genes: update 1998.

Lubs H, Chiurazzi P, Arena J, Schwartz C, Tranebjaerg L, Neri G.

Am J Med Genet. 1999 Apr 2;83(4):237-47. Review.

PMID:
10208155
6.

Renpenning syndrome maps to Xp11.

Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE.

Am J Hum Genet. 1998 May;62(5):1092-101.

7.

XLMR genes: update 1996.

Lubs HA, Chiurazzi P, Arena JF, Schwartz C, Tranebjaerg L, Neri G.

Am J Med Genet. 1996 Jul 12;64(1):147-57. Review.

PMID:
8826465
8.

Sixty years of X-linked mental retardation: a historical footnote.

Neri G, Opitz JM.

Am J Med Genet. 2000 Fall;97(3):228-33.

PMID:
11449492
9.

[Genetics of mental retardation].

Prieto García F.

Neurologia. 1998 May;13(5):218-22. Review. Spanish.

PMID:
9646628
10.

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 12;64(1):169-75. Review.

PMID:
8826469
11.

XLMR genes: update 1994.

Neri G, Chiurazzi P, Arena JF, Lubs HA.

Am J Med Genet. 1994 Jul 15;51(4):542-9. Review.

PMID:
7943038
12.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
13.

Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M.

Am J Med Genet. 1993 Apr 15;46(2):172-5.

PMID:
8484404
14.

X-linked mental retardation and neurological symptoms: a nosological approach.

Schrander-Stumpel CT, Höweler CJ, Fryns JP.

Genet Couns. 1995;6(1):21-32. Review.

PMID:
7794558
15.

A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.

Pai GS, Hane B, Joseph M, Nelson R, Hammond LS, Arena JF, Lubs HA, Stevenson RE, Schwartz CE.

J Med Genet. 1997 Jul;34(7):529-34.

16.

Monogenic causes of X-linked mental retardation.

Chelly J, Mandel JL.

Nat Rev Genet. 2001 Sep;2(9):669-80. Review.

PMID:
11533716
17.

Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.

Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F.

Am J Med Genet. 2001 Aug 1;102(2):200-4.

PMID:
11477616
18.

Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Strain L, Wright AF, Bonthron DT.

J Med Genet. 1997 Jul;34(7):535-40.

19.
20.

X-linked mental retardation: further lumping, splitting and emerging phenotypes.

Kleefstra T, Hamel BC.

Clin Genet. 2005 Jun;67(6):451-67. Review. Erratum in: Clin Genet. 2006 Feb;69(2):197.

PMID:
15857409
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk