Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 11

1.

Allan-Herndon syndrome--or X-linked cerebral palsy?

Bundey S, Comley LA, Blair A.

Am J Hum Genet. 1991 Jun;48(6):1214. No abstract available.

2.
3.

Cerebral palsy due to chromosomal anomalies and continuous gene syndromes.

Menkes JH, Flores-Sarnat L.

Clin Perinatol. 2006 Jun;33(2):481-501. Review.

PMID:
16765733
4.

Lethal multiple pterygium syndrome in four male fetuses in a family: evidence for an X-linked recessive subtype?

Meyer-Cohen J, Dillon A, Pai GS, Conradi S.

Am J Med Genet. 1999 Jan 1;82(1):97-9. Review. No abstract available.

PMID:
9916854
5.

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.

Dobyns WB, Berry-Kravis E, Havernick NJ, Holden KR, Viskochil D.

Am J Med Genet. 1999 Oct 8;86(4):331-7. Review.

PMID:
10494089
6.

Genetics considerations in cerebral palsy.

Schaefer GB.

Semin Pediatr Neurol. 2008 Mar;15(1):21-6. doi: 10.1016/j.spen.2008.01.004. Review.

PMID:
18342257
7.

Fragile X syndrome: a major cause of X-linked mental retardation.

Butler MG.

Compr Ther. 1988 Jul;14(7):3-7. Review. No abstract available.

PMID:
3060303
8.

X-linked immunodeficiencies.

Conley ME.

Curr Opin Genet Dev. 1994 Jun;4(3):401-6. Review.

PMID:
7919918
9.

[X-linked hydrocephalus syndrome].

Okamoto N.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):47-8. Review. Japanese. No abstract available.

PMID:
11057138
10.

Non-specific X-linked mental retardation: background, types, diagnosis and prevalence.

Howard-Peebles PN.

J Ment Defic Res. 1982 Dec;26 (Pt 4):205-13. Review.

PMID:
6763078
11.

[Molecular genetics of X-linked primary immunodeficiencies: advances in diagnosis and prevention].

Carbonara A, Brusco A, Carbonara C.

Ann Ital Med Int. 1996 Jul-Sep;11(3):180-6. Review. Italian.

PMID:
8998263

Supplemental Content

Support Center