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Results: 1 to 20 of 95

1.

Neonatal X-linked hydrocephalus. Findings in two affected brothers.

Habib Z.

Hereditas. 1979;91(1):79-82. No abstract available.

PMID:
500393
[PubMed - indexed for MEDLINE]
2.

Familial hydrocephalus of prenatal onset.

Zlotogora J, Sagi M, Cohen T.

Am J Med Genet. 1994 Jan 15;49(2):202-4.

PMID:
8116668
[PubMed - indexed for MEDLINE]
3.

[X chromosome recessively transmitted hydrocephalus with congenital aqueduct stenosis].

Reinthaller A, Deutinger J.

Z Geburtshilfe Perinatol. 1985 Sep-Oct;189(5):244-6. German.

PMID:
3907171
[PubMed - indexed for MEDLINE]
4.

Genetics and genetic counselling in neonatal hydrocephalus.

Habib Z.

Obstet Gynecol Surv. 1981 Oct;36(10):529-34. Review.

PMID:
7029366
[PubMed - indexed for MEDLINE]
5.

The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families.

Schrander-Stumpel C, Meyer H, Merckx D, Jones M, Israel J, Sommer A, Stevens C, Tinschert S, Wilson G, Willems P, et al.

Genet Couns. 1994;5(1):1-10.

PMID:
8031529
[PubMed - indexed for MEDLINE]
6.

[X chronmosome-linked hydrocephalus. Diagnostic and genetic-counseling aspects].

Kocoń-Sladowska H, Sito A, Maślińska D.

Pediatr Pol. 1980 Apr;55(4):463-71. Polish. No abstract available.

PMID:
7191083
[PubMed - indexed for MEDLINE]
7.

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia.

Halliday J, Chow CW, Wallace D, Danks DM.

J Med Genet. 1986 Feb;23(1):23-31.

PMID:
3950933
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

[X-linked congenital hydrocephalus. Description of a case].

Spada A, De Marchi M, Mellano G.

Minerva Pediatr. 1978 Jun 30;30(12):1033-7. Italian. No abstract available.

PMID:
566846
[PubMed - indexed for MEDLINE]
9.

Sex linked hydrocephalus.

Cassie R, Boon AR.

J Med Genet. 1977 Feb;14(1):72-3.

PMID:
839507
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Strain L, Gosden CM, Brock DJ, Bonthron DT.

Am J Hum Genet. 1994 Feb;54(2):236-43.

PMID:
8304340
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

X-linked hydrocephalus.

Shannon MW, Nadler HL.

J Med Genet. 1968 Dec;5(4):326-8. No abstract available.

PMID:
5713648
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

X-linked congenital hydrocephalus.

Renier WO, Ter Haar BG, Slooff JL, Hustinx TW, Gabreëls FJ.

Clin Neurol Neurosurg. 1982;84(2):113-23.

PMID:
6288305
[PubMed - indexed for MEDLINE]
13.

Casey Holter Essay Prize. The pathogenesis of X-linked hydrocephalus.

Jouet M.

Eur J Pediatr Surg. 1995 Dec;5 Suppl 1:5-7. Review. No abstract available.

PMID:
8770568
[PubMed - indexed for MEDLINE]
14.

X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one family.

Brewer CM, Fredericks BJ, Pont JM, Stephenson JB, Tolmie JL.

Dev Med Child Neurol. 1996 Jul;38(7):632-6.

PMID:
8674913
[PubMed - indexed for MEDLINE]
15.

Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28.

Gigarel N, Frydman N, Burlet P, Kerbrat V, Steffann J, Frydman R, Munnich A, Ray PF.

Hum Genet. 2004 Feb;114(3):298-305. Epub 2003 Dec 12.

PMID:
14673643
[PubMed - indexed for MEDLINE]
16.

Recurrence risk in hydrocephalus.

Bay C, Kerzin L, Hall BD.

Birth Defects Orig Artic Ser. 1979;15(5C):95-105. No abstract available.

PMID:
526618
[PubMed - indexed for MEDLINE]
17.

[Prenatal diagnosis of X-linked hydrocephalus].

Mikiel-Kostyra K, Dipont T.

Ginekol Pol. 1983 Aug-Sep;54(8-9):549-52. Polish. No abstract available.

PMID:
6667886
[PubMed - indexed for MEDLINE]
18.

Case report; A case of 4P.-syndrome and a family of X-linked hydrocephalus.

Odo S, Ogata H, Kamisasanuki S, Ikeda T.

Jinrui Idengaku Zasshi. 1974 Jun;19(1):76-7. No abstract available.

PMID:
4476857
[PubMed - indexed for MEDLINE]
19.

VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.

Wang H, Hunter AG, Clifford B, McLaughlin M, Thompson D.

Am J Med Genet. 1993 Aug 1;47(1):114-7.

PMID:
8368240
[PubMed - indexed for MEDLINE]
20.

[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?].

Sengers RC, Hamel BC, Otten BJ, van Gils JF, de Pagter AG.

Tijdschr Kindergeneeskd. 1985 Feb;53(1):31-4. Dutch.

PMID:
4039476
[PubMed - indexed for MEDLINE]

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