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Results: 1 to 20 of 149

Related Citations for PubMed (Select 2878939)

1.
2.

Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment.

Reilly DS, Lewis RA, Ledbetter DH, Nussbaum RL.

Am J Hum Genet. 1988 May;42(5):748-55.

4.

Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndrome.

Reilly DS, Lewis RA, Nussbaum RL.

Genomics. 1990 Sep;8(1):62-70.

PMID:
2081601
5.

Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint.

Mueller OT, Hartsfield JK Jr, Gallardo LA, Essig YP, Miller KL, Papenhausen PR, Tedesco TA.

Am J Hum Genet. 1991 Oct;49(4):804-10.

6.

Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.

Hittner HM, Carroll AJ, Prchal JT.

Am J Hum Genet. 1982 Nov;34(6):966-71.

7.

Prenatal diagnosis of Löwe's syndrome: a case report with evidence of de novo mutation.

Gazit E, Brand N, Harel Y, Lotan D, Barkai G.

Prenat Diagn. 1990 Apr;10(4):257-60. No abstract available.

PMID:
1973295
8.

A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome.

Hodgson SV, Heckmatt JZ, Hughes E, Crolla JA, Dubowitz V, Bobrow M.

Am J Med Genet. 1986 Mar;23(3):837-47.

PMID:
3953680
9.

Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.

Nussbaum RL, Lewis RA, Lesko JG, Ferrell R.

Am J Hum Genet. 1985 May;37(3):473-81.

10.

[The Lyon effect of the lens: findings in the carriers of X chromosome-linked cataract and in Lowe syndrome].

Koniszewski G, Rott HD.

Klin Monbl Augenheilkd. 1985 Dec;187(6):525-8. German.

PMID:
4094364
11.
12.

Mapping the X-linked lymphoproliferative syndrome.

Skare JC, Milunsky A, Byron KS, Sullivan JL.

Proc Natl Acad Sci U S A. 1987 Apr;84(7):2015-8.

13.

[Oculocerebrorenal syndrome in a girl].

Frézal J, Hors-Cayla MC, Szpiro-Tapia S.

Arch Fr Pediatr. 1986 Aug-Sep;43(7):537. French. No abstract available.

PMID:
3800569
14.

[Sex-related neurologic diseases. Duchenne muscular dystrophy. Lowe's disease].

Castro-Gago M.

An Esp Pediatr. 1984 Oct;21 Suppl 20:51-4. Spanish. No abstract available.

PMID:
6517412
15.

Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.

Sylla BS, Wang Q, Hayoz D, Lathrop GM, Lenoir GM.

Clin Genet. 1989 Dec;36(6):459-62.

PMID:
2574086
16.

Mapping of the X-linked recessive retinitis pigmentosa gene. A review.

Musarella MA.

Ophthalmic Paediatr Genet. 1990 Jun;11(2):77-88. Review.

PMID:
1974043
17.

Linkage analyses in families with nephrogenic diabetes insipidus.

Knoers NV, van der Heyden H, van Oost BA, Monnens L, Willems J, Ropers HH.

Prog Clin Biol Res. 1989;305:149-55. No abstract available.

PMID:
2569742
19.

Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.

Brown WT, Ye W, Gross AC, Chan CB, Dobkin CS, Jenkins EC.

Am J Med Genet. 1988 May-Jun;30(1-2):551-66.

PMID:
2902796
20.

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

Yates JR, Affara NA, Jamieson DM, Ferguson-Smith MA, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Johnston AW, Kelly K.

J Med Genet. 1986 Dec;23(6):587-90.

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