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Results: 1 to 20 of 102

1.

Fine mapping of the chicken congenital loco locus on chromosome 12.

Okumura Y, Ohtake T, Uemoto Y, Sato S, Sato S, Kobayashi E.

Anim Genet. 2013 Dec;44(6):778-81. doi: 10.1111/age.12065. Epub 2013 Jun 7.

PMID:
23742667
[PubMed - indexed for MEDLINE]
2.

Sequence analysis of a pea comb locus on chicken chromosome 1.

Sato S, Sato S, Otake T, Suzuki C, Uemoto Y, Saburi J, Hashimoto H, Kobayashi E.

Anim Genet. 2010 Dec;41(6):659-61. doi: 10.1111/j.1365-2052.2010.02048.x.

PMID:
20412124
[PubMed - indexed for MEDLINE]
3.

Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p.

Sabir N, Riazuddin SA, Kaul H, Iqbal F, Nasir IA, Zafar AU, Qazi ZA, Butt NH, Khan SN, Husnain T, Hejtmancik JF, Riazuddin S.

Mol Vis. 2010 Dec 30;16:2911-5.

PMID:
21203409
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Localization of the muscular dystrophy AM locus using a chicken linkage map constructed with the Kobe University resource family.

Lee EJ, Yoshizawa K, Mannen H, Kikuchi H, Kikuchi T, Mizutani M, Tsuji S.

Anim Genet. 2002 Feb;33(1):42-8.

PMID:
11849136
[PubMed - indexed for MEDLINE]
5.

Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q.

Sabir N, Riazuddin SA, Butt T, Iqbal F, Nasir IA, Zafar AU, Qazi ZA, Butt NH, Khan SN, Husnain T, Hejtmancik JF, Riazuddin S.

Mol Vis. 2010 Dec 8;16:2634-8.

PMID:
21179239
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p.

Naz S, Riazuddin SA, Li L, Shahid M, Kousar S, Sieving PA, Hejtmancik JF, Riazuddin S.

Am J Ophthalmol. 2010 May;149(5):861-6. doi: 10.1016/j.ajo.2009.12.034. Epub 2010 Mar 15.

PMID:
20227676
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genetic mapping of quantitative trait loci affecting susceptibility in chicken to develop pulmonary hypertension syndrome.

Rabie TS, Crooijmans RP, Bovenhuis H, Vereijken AL, Veenendaal T, van der Poel JJ, Van Arendonk JA, Pakdel A, Groenen MA.

Anim Genet. 2005 Dec;36(6):468-76.

PMID:
16293119
[PubMed - indexed for MEDLINE]
8.

Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.

Masmoudi S, Charfedine I, Rebeh IB, Rebai A, Tlili A, Ghorbel AM, Belguith H, Petit C, Drira M, Ayadi H.

Clin Genet. 2004 Oct;66(4):358-64.

PMID:
15355440
[PubMed - indexed for MEDLINE]
9.

Relationship between microsatellite marker alleles on chromosomes 1-5 originating from the Rhode Island Red and Green-legged Partrigenous breeds and egg production and quality traits in F(2) mapping population.

Wardecka B, Olszewski R, Jaszczak K, Zieba G, Pierzchała M, Wicińska K.

J Appl Genet. 2002;43(3):319-29.

PMID:
12177521
[PubMed - indexed for MEDLINE]
10.

Mapping of the recessive white locus and analysis of the tyrosinase gene in chickens.

Sato S, Otake T, Suzuki C, Saburi J, Kobayashi E.

Poult Sci. 2007 Oct;86(10):2126-33.

PMID:
17878441
[PubMed - indexed for MEDLINE]
11.

Linkage mapping of the locus responsible for congenital multiple ocular defects in cattle on bovine Chromosome 18.

Abbasi AR, Ihara N, Watanabe T, Khalaj M, Tsuji T, Sugimoto Y, Kunieda T.

Mamm Genome. 2005 Sep;16(9):731-7. Epub 2005 Oct 20.

PMID:
16245030
[PubMed - indexed for MEDLINE]
12.

A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.

Riazuddin SA, Yasmeen A, Zhang Q, Yao W, Sabar MF, Ahmed Z, Riazuddin S, Hejtmancik JF.

Invest Ophthalmol Vis Sci. 2005 Feb;46(2):623-6.

PMID:
15671291
[PubMed - indexed for MEDLINE]
Free Article
13.

Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes.

Bejaoui K, Liu J, McKenna-Yasek D, Le Paslier D, Bossie K, Gilligan DM, Brown RH.

Neurogenetics. 1998 Mar;1(3):189-96.

PMID:
10737122
[PubMed - indexed for MEDLINE]
14.
15.

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H.

Genet Med. 2005 Jul-Aug;7(6):397-405.

PMID:
16024971
[PubMed - indexed for MEDLINE]
16.

A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.

Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y.

Mol Vis. 2007 Aug 1;13:1357-62.

PMID:
17768382
[PubMed - indexed for MEDLINE]
Free Article
17.

A first-generation microsatellite-based genetic linkage map of the Siberian jay (Perisoreus infaustus): insights into avian genome evolution.

Jaari S, Li MH, Merilä J.

BMC Genomics. 2009 Jan 3;10:1. doi: 10.1186/1471-2164-10-1.

PMID:
19121221
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.

Yang Z, Xiao X, Li S, Zhang Q.

Mol Vis. 2009;15:312-8. Epub 2009 Feb 9.

PMID:
19204786
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.

Hadj-Rabia S, Salomon R, Pelet A, Penet C, Rotschild A, de Laët MH, Chaouachi B, Hannachi R, Bakiri F, Brauner R, Chaussain JL, Munnich A, Lyonnet S.

Eur J Hum Genet. 2000 Aug;8(8):613-20.

PMID:
10951524
[PubMed - indexed for MEDLINE]
Free Article
20.

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.

Masmoudi S, Tlili A, Majava M, Ghorbel AM, Chardenoux S, Lemainque A, Zina ZB, Moala J, Männikkö M, Weil D, Lathrop M, Ala-Kokko L, Drira M, Petit C, Ayadi H.

Eur J Hum Genet. 2003 Feb;11(2):185-8.

PMID:
12634867
[PubMed - indexed for MEDLINE]
Free Article

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