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Items: 1 to 20 of 28

1.

A new MRXS locus maps to the X chromosome pericentromeric region: a new syndrome or narrow definition of Sutherland-Haan genetic locus?

Fichera M, Borgione E, Avola E, Amata S, Sturnio M, Romano C, Ragusa A.

J Med Genet. 2002 Apr;39(4):276-80. No abstract available.

2.

Nomenclature guidelines for X-linked mental retardation.

Mulley JC, Kerr B, Stevenson R, Lubs H.

Am J Med Genet. 1992 Apr 15-May 1;43(1-2):383-91. Review.

PMID:
1605216
3.

Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21.

Häne B, Schroer RJ, Arena JF, Lubs HA, Schwartz CE, Stevenson RE.

Clin Genet. 1996 Oct;50(4):176-83. Review.

PMID:
9001795
4.

Syndromic XLMR genes (MRXS): update 2000.

Hamel BC, Chiurazzi P, Lubs HA.

Am J Med Genet. 2000 Oct 23;94(5):361-3. Review. No abstract available.

PMID:
11050617
5.

MRX review.

Chelly J.

Am J Med Genet. 2000 Oct 23;94(5):364-6. Review. No abstract available.

PMID:
11050618
6.
7.

In search of the MRX genes.

Toniolo D.

Am J Med Genet. 2000 Fall;97(3):221-7. Review.

PMID:
11449491
8.

[Börjeson-Forssman-Lehmann syndrome].

Fujieda K.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):147-9. Review. Japanese. No abstract available.

PMID:
11057174
9.

X-linked mental retardation.

Neri G, Chiurazzi P.

Adv Genet. 1999;41:55-94. Review. No abstract available.

PMID:
10494617
10.

Application of linked markers for genetic diagnosis of Alport syndrome.

Barker DF, Atkin CL, Gregory MC, Fain PR.

Contrib Nephrol. 1996;117:29-45. Review. No abstract available.

PMID:
8801047
11.

[Danon disease].

Nishino I.

Ryoikibetsu Shokogun Shirizu. 2001;(36):225-9. Review. Japanese. No abstract available.

PMID:
11596375
12.
13.

[Recent advances in the genetics and physiopathology of X chromosomal mental retardation].

Chelly J.

Arch Pediatr. 2000 May;7 Suppl 2:114s-118s. Review. French. No abstract available.

PMID:
10904677
14.

[Coffin-Lowry syndrome].

Ishii T.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):163-5. Review. Japanese. No abstract available.

PMID:
11057180
15.

Epileptogenesis: clinical genetic and genetic epidemiologic aspects.

Lindhout D.

Epilepsy Res Suppl. 1996;12:21-30. Review. No abstract available.

PMID:
9302500
16.

[X-linked mental retardation syndromes].

Kurosawa K.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):123-30. Review. Japanese. No abstract available.

PMID:
11057166
17.

Mapping of the loci for mental retardation syndromes in the distal Xq.

Schmidt M.

Am J Med Genet. 1996 Jul 12;64(1):163-5. Review. No abstract available.

PMID:
8826467
18.

[Lujan-Fryns syndrome].

Izumikawa Y.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):117. Review. Japanese. No abstract available.

PMID:
11528648
19.
20.

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060.

Barth PG, Wanders RJ, Vreken P.

J Pediatr. 1999 Sep;135(3):273-6. Review. No abstract available.

PMID:
10484787
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