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Results: 1 to 20 of 87

1.

Current status of human chromosome 14.

Kamnasaran D, Cox DW.

J Med Genet. 2002 Feb;39(2):81-90. Review.

PMID:
11836355
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Epigenetic inheritance associated with human chromosome 14.

Kamnasaran D.

Clin Invest Med. 2001 Jun;24(3):138-46. Review. Erratum in: Clin Invest Med 2001 Aug;24(4):178.

PMID:
11437065
[PubMed - indexed for MEDLINE]
3.

An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the 'Legs at odd angles' (Loa) mutation.

Witherden AS, Hafezparast M, Nicholson SJ, Ahmad-Annuar A, Bermingham N, Arac D, Rankin J, Iravani M, Ball S, Peters J, Martin JE, Huntley D, Hummerich H, Sergot M, Fisher EM.

Gene. 2002 Jan 23;283(1-2):71-82.

PMID:
11867214
[PubMed - indexed for MEDLINE]
4.

Uniparental disomy and genomic imprinting as causes of human genetic disease.

Cassidy SB.

Environ Mol Mutagen. 1995;25 Suppl 26:13-20. Review.

PMID:
7789357
[PubMed - indexed for MEDLINE]
5.

Linkage analysis of adult height with parent-of-origin effects in the Framingham Heart Study.

Mukhopadhyay N, Weeks DE; Framingham Heart Study.

BMC Genet. 2003 Dec 31;4 Suppl 1:S76.

PMID:
14975144
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Comparative mapping of human chromosome 10 to pig chromosomes 10 and 14.

Nonneman D, Rohrer GA.

Anim Genet. 2004 Aug;35(4):338-43.

PMID:
15265077
[PubMed - indexed for MEDLINE]
7.

A case of segmental paternal isodisomy of chromosome 14.

Coveler KJ, Yang SP, Sutton R, Milstein JM, Wu YQ, Bois KD, Beischel LS, Johnson JP, Shaffer LG.

Hum Genet. 2002 Mar;110(3):251-6. Epub 2002 Feb 26. Review.

PMID:
11935337
[PubMed - indexed for MEDLINE]
8.

Genetic analysis of psychiatric disorders associated with human chromosome 18.

Kamnasaran D.

Clin Invest Med. 2003 Dec;26(6):285-302. Review.

PMID:
14690303
[PubMed - indexed for MEDLINE]
9.

Cytogenetic anchoring of radiation hybrid and virtual maps of sheep chromosome X and comparison of X chromosomes in sheep, cattle, and human.

Goldammer T, Brunner RM, Rebl A, Wu CH, Nomura K, Hadfield T, Maddox JF, Cockett NE.

Chromosome Res. 2009;17(4):497-506. doi: 10.1007/s10577-009-9047-9. Epub 2009 Jul 3.

PMID:
19575301
[PubMed - indexed for MEDLINE]
10.

[Evaluation of the role of uniparental disomy in early embryolethality of man].

Nikitina TV, Sazhenova EA, Sukhanova NN, Lebedev IN, Nazarenko SA.

Ontogenez. 2004 Jul-Aug;35(4):297-306. Russian.

PMID:
15487349
[PubMed - indexed for MEDLINE]
11.

Comparative sequence analysis of imprinted genes between human and mouse to reveal imprinting signatures.

Wang Z, Fan H, Yang HH, Hu Y, Buetow KH, Lee MP.

Genomics. 2004 Mar;83(3):395-401.

PMID:
14962665
[PubMed - indexed for MEDLINE]
12.

Comparative mapping of Homo sapiens chromosome 4 (HSA4) and Sus scrofa chromosome 8 (SSC8) using orthologous genes representing different cytogenetic bands as landmarks.

Jiang Z, He H, Hamasima N, Suzuki H, Verrinder G.

Genome. 2002 Feb;45(1):147-56.

PMID:
11908657
[PubMed - indexed for MEDLINE]
13.

High-resolution comprehensive radiation hybrid maps of the porcine chromosomes 2p and 9p compared with the human chromosome 11.

Liu WS, Yasue H, Eyer K, Hiraiwa H, Shimogiri T, Roelofs B, Landrito E, Ekstrand J, Treat M, Paes N, Lemos M, Griffith AC, Davis ML, Meyers SN, Yerle M, Milan D, Beever JE, Schook LB, Beattie CW.

Cytogenet Genome Res. 2008;120(1-2):157-63. doi: 10.1159/000118757. Epub 2008 Apr 30.

PMID:
18467842
[PubMed - indexed for MEDLINE]
14.

Targeted construction of a high-resolution, integrated, comprehensive, and comparative map for a region specific to bovine chromosome 6 based on radiation hybrid mapping.

Weikard R, Kühn C, Goldammer T, Laurent P, Womack JE, Schwerin M.

Genomics. 2002 Jun;79(6):768-76.

PMID:
12036290
[PubMed - indexed for MEDLINE]
15.

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.

Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.

Mov Disord. 2006 Jan;21(1):28-33.

PMID:
16124010
[PubMed - indexed for MEDLINE]
16.

Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion.

Tsukishiro S, Li QY, Tanemura M, Sugiura-Ogasawara M, Suzumori K, Sonta S.

J Hum Genet. 2005;50(3):112-7. Epub 2005 Mar 4.

PMID:
15747166
[PubMed - indexed for MEDLINE]
17.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
[PubMed - indexed for MEDLINE]
18.

A high-resolution comparative radiation hybrid map of ovine chromosomal regions that are homologous to human chromosome 6 (HSA6).

Wu CH, Nomura K, Goldammer T, Hadfield T, Dalrymple BP, McWilliam S, Maddox JF, Womack JE, Cockett NE.

Anim Genet. 2008 Oct;39(5):459-67. doi: 10.1111/j.1365-2052.2008.01751.x. Epub 2008 Jun 28.

PMID:
18565162
[PubMed - indexed for MEDLINE]
19.

Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype.

Chu C, Schwartz S, McPherson E.

Am J Med Genet A. 2004 Jun 1;127A(2):167-71.

PMID:
15108205
[PubMed - indexed for MEDLINE]
20.

Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12).

Sutton VR, McAlister WH, Bertin TK, Kaffe S, Wang JC, Yano S, Shaffer LG, Lee B, Epstein CJ, Villar AJ.

Hum Genet. 2003 Oct;113(5):447-51. Epub 2003 Aug 21.

PMID:
12938037
[PubMed - indexed for MEDLINE]

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