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Items: 1 to 20 of 145

1.

Hypopigmentation in the Prader-Willi syndrome.

Wiesner GL, Bendel CM, Olds DP, White JG, Arthur DC, Ball DW, King RA.

Am J Hum Genet. 1987 May;40(5):431-42.

2.
3.

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele.

Spritz RA, Bailin T, Nicholls RD, Lee ST, Park SK, Mascari MJ, Butler MG.

Am J Med Genet. 1997 Jul 11;71(1):57-62.

PMID:
9215770
4.

Hypopigmentation in Angelman syndrome.

King RA, Wiesner GL, Townsend D, White JG.

Am J Med Genet. 1993 Apr 1;46(1):40-4.

PMID:
8494033
5.

Visual evoked potentials in Prader-Willi syndrome.

Apkarian P, Spekreijse H, van Swaay E, van Schooneveld M.

Doc Ophthalmol. 1989 Apr;71(4):355-67.

PMID:
2791841
6.

Prader-Willi syndrome: current understanding of cause and diagnosis.

Butler MG.

Am J Med Genet. 1990 Mar;35(3):319-32.

PMID:
2309779
7.

[Self-induced cutaneous lesions in Prader-Willi syndrome].

Plantin P, Milochau P, Broussine L, Blondin G.

Ann Dermatol Venereol. 1997;124(5):390-2. French.

PMID:
9739896
8.

Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome.

Hittner HM, King RA, Riccardi VM, Ledbetter DH, Borda RP, Ferrell RE, Kretzer FL.

Am J Ophthalmol. 1982 Sep;94(3):328-37.

PMID:
6812426
9.

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.

Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T.

Pediatrics. 2004 Mar;113(3 Pt 1):565-73.

PMID:
14993551
10.

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Butler MG, Meaney FJ, Palmer CG.

Am J Med Genet. 1986 Mar;23(3):793-809.

PMID:
3953677
11.

A neuropathological study of a case of the Prader-Willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15.

Hayashi M, Itoh M, Kabasawa Y, Hayashi H, Satoh J, Morimatsu Y.

Brain Dev. 1992 Jan;14(1):58-62.

PMID:
1590529
12.

Interstitial 6q deletion and Prader-Willi-like phenotype.

Stein CK, Stred SE, Thomson LL, Smith FC, Hoo JJ.

Clin Genet. 1996 Jun;49(6):306-10.

PMID:
8884080
13.

Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.

Creel DJ, Bendel CM, Wiesner GL, Wirtschafter JD, Arthur DC, King RA.

N Engl J Med. 1986 Jun 19;314(25):1606-9.

PMID:
3713758
14.

Duplication of proximal 15q as a cause of Prader-Willi syndrome.

Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH.

Am J Med Genet. 1987 Dec;28(4):791-802.

PMID:
3688017
15.

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.

Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S.

Am J Med Genet. 1997 Feb 11;68(4):433-40.

PMID:
9021017
16.

The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2.

Brilliant MH, King R, Francke U, Schuffenhauer S, Meitinger T, Gardner JM, Durham-Pierre D, Nakatsu Y.

Pigment Cell Res. 1994 Dec;7(6):398-402.

PMID:
7761348
17.

Deletions of proximal 15q without Prader-Willi syndrome.

Greenberg F, Ledbetter DH.

Am J Med Genet. 1987 Dec;28(4):813-20.

PMID:
3688019
18.

Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).

Erdel M, Schuffenhauer S, Buchholz B, Barth-Witte U, Köchl S, Utermann B, Duba HC, Utermann G.

Hum Genet. 1996 Jun;97(6):784-93.

PMID:
8641697
19.
20.

[Prader-Willi syndrome associated with chromosomal aberration: report of a case].

Kokura K, Shima H, Mori Y, Ikoma F, Sakamoto H, Furuyama J.

Hinyokika Kiyo. 1992 Sep;38(9):1079-82. Japanese.

PMID:
1357945
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