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Items: 1 to 20 of 23

1.

The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigrees.

Claes S, Devriendt K, Lagae L, Ceulemans B, Dom L, Casaer P, Raeymaekers P, Cassiman JJ, Fryns JP.

Ann Neurol. 1997 Sep;42(3):360-4.

PMID:
9307258
2.

[Aicardi's syndrome: agenesis of the corpus callosum, infantile flexor spasms and macular dystrophy].

Badalian LO, Medvedev MI, Berestov AI, Kharlamov DA, Lysov VL.

Zh Nevrol Psikhiatr Im S S Korsakova. 1996;96(5):87-90. Review. Russian. No abstract available.

PMID:
9012263
3.

Inherited enamel defects.

Bäckman B.

Ciba Found Symp. 1997;205:175-82; discussion 183-6. Review.

PMID:
9189624
4.

Molecular approaches to the Rett syndrome gene.

Schanen NC.

J Child Neurol. 1999 Dec;14(12):806-14. Review.

PMID:
10614568
5.

Genetic considerations in childhood epilepsy.

Bird TD.

Epilepsia. 1987;28 Suppl 1:S71-81. Review.

PMID:
3113931
6.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
7.

The eye and the chromosome.

Mets MB, Maumenee IH.

Surv Ophthalmol. 1983 Jul-Aug;28(1):20-32. Review.

PMID:
6353648
8.

[Genetic causes of infantile spasms--a systematic review].

Hansen LK, Ousager LB, Møller RS, Uldall PV, Hjalgrim H.

Ugeskr Laeger. 2012 Apr 23;174(17):1152-5. Review. Danish.

PMID:
22533931
9.

Genetic aspects of Rett syndrome.

Zoghbi H.

J Child Neurol. 1988;3 Suppl:S76-8. Review.

PMID:
3058791
10.

[Disposition toward mood genes].

Guedj F.

Encephale. 1997 Jan;23 Spec No 1:2-6. Review. French.

PMID:
9172974
11.

The recognition and investigation of X-linked learning disability syndromes.

Feldman EJ.

J Intellect Disabil Res. 1996 Oct;40 ( Pt 5):400-11. Review.

PMID:
8906528
12.

Analysing human developmental abnormalities.

Winter RM.

Bioessays. 1996 Dec;18(12):965-71. Review.

PMID:
8976153
13.

[Heritable X-chromosome disease].

de la Chapelle A.

Duodecim. 1988;104(22):1774-86. Review. Finnish. No abstract available.

PMID:
3065062
14.

[Research advance in the etiology of West syndrome].

Liu ZL, Zou LP.

Zhongguo Dang Dai Er Ke Za Zhi. 2010 Feb;12(2):159-61. Review. Chinese. No abstract available.

15.

Familial correlational analyses, sex differences, and the X-linked gene hypothesis.

Thomas H.

Psychol Bull. 1983 May;93(3):427-40. Review. No abstract available.

PMID:
6346370
16.

Molecular dissection of genetic diseases of brain and muscle.

Nicholson GA.

Med J Aust. 1993 Jul 5;159(1):52-4. Review. No abstract available.

PMID:
8316117
17.

Microcytogenetics of chromosome X.

Ioan DM, Ghergar D, Pop T.

Endocrinologie. 1989 Jul-Sep;27(3):191-4. Review. No abstract available.

PMID:
2683015
18.

Craniosynostosis in X-linked hypophosphataemic rickets.

Willis FR, Beattie TJ.

J Paediatr Child Health. 1997 Feb;33(1):78-9. Review.

PMID:
9069051
19.

The X chromosome and ovarian function.

Vialard F, Cocquet J, Christin-Maitre S, Veitia R, Fellous M.

Cytogenet Genome Res. 2002;99(1-4):218-23. Review. No abstract available.

PMID:
12900567
20.

Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12.

Gerald PS, Grzeschik KH.

Cytogenet Cell Genet. 1984;37(1-4):103-26. Review. No abstract available.

PMID:
6360555
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