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Items: 1 to 20 of 354

1.

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.

2.

Renpenning syndrome comes into focus.

Stevenson RE, Bennett CW, Abidi F, Kleefstra T, Porteous M, Simensen RJ, Lubs HA, Hamel BC, Schwartz CE.

Am J Med Genet A. 2005 May 1;134(4):415-21.

PMID:
15782410
3.

Linkage analysis in three families with nonspecific X-linked mental retardation.

Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P.

Am J Med Genet. 1996 Jul 12;64(1):137-46.

PMID:
8826464
4.

Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2.

Bar-David S, Lerer I, Sarfaty CK, Kohan ZG, Meiner V, Zlotogora J, Abeliovich D.

Am J Med Genet. 1996 Jul 12;64(1):83-8.

PMID:
8826456
5.

Allan-Herndon syndrome. I. Clinical studies.

Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT Jr, Herndon CN.

Am J Hum Genet. 1990 Sep;47(3):446-53.

6.
7.

Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24.

des Portes V, Soufir N, Carrié A, Billuart P, Bienvenu T, Vinet MC, Beldjord C, Ponsot G, Kahn A, Boué J, Chelly J.

Am J Med Genet. 1997 Oct 31;72(3):324-8.

PMID:
9332663
8.

Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.

Martínez F, Martínez-Garay I, Oltra S, Moltó MD, Orellana C, Monfort S, Prieto F, Tejada I.

Am J Med Genet A. 2004 Dec 1;131(2):174-8.

PMID:
15526294
9.

Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1.

Guo X, Shen H, Xiao X, Dai Q, Li S, Jia X, Hejtmancik JF, Zhang Q.

J Hum Genet. 2006;51(8):695-700. Epub 2006 Jul 11.

PMID:
16832577
11.

Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54).

Jemaa LB, des Portes V, Zemni R, Mrad R, Maazoul F, Beldjord C, Chaabouni H, Chelly J.

Am J Med Genet. 1999 Jul 30;85(3):276-82.

PMID:
10398243
12.

X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families).

Archidiacono N, Rocchi M, Rinaldi A, Filippi G.

J Genet Hum. 1987 Dec;35(5):381-98.

PMID:
3437266
13.

X-linked alpha-thalassemia/mental retardation syndrome. Linkage analysis in a new family further supports localization in proximal Xq.

Houdayer CI, Toutain A, Ronce N, Lefort G, Sarda P, Taib J, Briault S, Lambert JC, Moraine CI.

Ann Genet. 1993;36(4):194-9.

PMID:
8166423
14.

X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.

Gendrot C, Ronce N, Toutain A, Moizard MP, Müh JP, Raynaud M, Dourlens J, Briault S, Moraine C.

Clin Genet. 1994 Mar;45(3):145-53.

PMID:
8026106
15.

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.

Tahvanainen E, Norio R, Karila E, Ranta S, Weissenbach J, Sistonen P, de la Chapelle A.

Nat Genet. 1994 Jun;7(2):201-4.

PMID:
7920642
16.
17.

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
18.

X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.

Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.

Am J Med Genet. 1999 Jul 30;85(3):216-20.

PMID:
10398231
19.

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
20.

X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12.

Arena JF, Schwartz C, Ouzts L, Stevenson R, Miller M, Garza J, Nance M, Lubs H.

Am J Med Genet. 1996 Jul 12;64(1):50-8.

PMID:
8826448

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