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Results: 15

References for PMC Articles for PubMed (Select 18680190)

1.

Transcriptome analysis of the murine forelimb and hindlimb autopod.

Shou S, Scott V, Reed C, Hitzemann R, Stadler HS.

Dev Dyn. 2005 Sep;234(1):74-89.

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3.

HaploPainter: a tool for drawing pedigrees with complex haplotypes.

Thiele H, Nürnberg P.

Bioinformatics. 2005 Apr 15;21(8):1730-2. Epub 2004 Sep 17.

4.

Prediction of mammalian microRNA targets.

Lewis BP, Shih IH, Jones-Rhoades MW, Bartel DP, Burge CB.

Cell. 2003 Dec 26;115(7):787-98.

PMID:
14697198
5.

Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family.

Ghadami M, Majidzadeh-A K, Haerian BS, Damavandi E, Yamada K, Pasallar P, Najafi MT, Nishimura G, Tomita HA, Yoshiura KI, Niikawa N.

Am J Med Genet. 2001 Nov 22;104(2):147-51.

PMID:
11746046
6.

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Abecasis GR, Cherny SS, Cookson WO, Cardon LR.

Nat Genet. 2002 Jan;30(1):97-101. Epub 2001 Dec 3.

PMID:
11731797
7.

Craniosynostosis and related limb anomalies.

Wilkie AO, Oldridge M, Tang Z, Maxson RE Jr.

Novartis Found Symp. 2001;232:122-33; discussion 133-43. Review.

PMID:
11277076
8.

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

Bosse K, Betz RC, Lee YA, Wienker TF, Reis A, Kleen H, Propping P, Cichon S, Nöthen MM.

Am J Hum Genet. 2000 Aug;67(2):492-7. Epub 2000 Jun 30.

9.
10.

Allele-sharing models: LOD scores and accurate linkage tests.

Kong A, Cox NJ.

Am J Hum Genet. 1997 Nov;61(5):1179-88.

11.

Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes.

Yoshiura K, Leysens NJ, Chang J, Ward D, Murray JC, Muenke M.

Am J Med Genet. 1997 Oct 31;72(3):354-62.

PMID:
9332670
12.

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

Muenke M, Gripp KW, McDonald-McGinn DM, Gaudenz K, Whitaker LA, Bartlett SP, Markowitz RI, Robin NH, Nwokoro N, Mulvihill JJ, Losken HW, Mulliken JB, Guttmacher AE, Wilroy RS, Clarke LA, Hollway G, Adès LC, Haan EA, Mulley JC, Cohen MM Jr, Bellus GA, Francomano CA, Moloney DM, Wall SA, Wilkie AO, et al.

Am J Hum Genet. 1997 Mar;60(3):555-64.

13.
14.

Parametric and nonparametric linkage analysis: a unified multipoint approach.

Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES.

Am J Hum Genet. 1996 Jun;58(6):1347-63.

15.

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

Wilkie AO, Slaney SF, Oldridge M, Poole MD, Ashworth GJ, Hockley AD, Hayward RD, David DJ, Pulleyn LJ, Rutland P, et al.

Nat Genet. 1995 Feb;9(2):165-72.

PMID:
7719344
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