Schutte BC - Search Results

1

The many faces and factors of orofacial clefts.

Schutte BC, Murray JC. Schutte BC, et al. Hum Mol Genet. 1999;8(10):1853-9. doi: 10.1093/hmg/8.10.1853. Hum Mol Genet. 1999. PMID: 10469837 Review.

2

Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.

Schutte BC, Sander A, Malik M, Murray JC. Schutte BC, et al. Genomics. 1996 Sep 15;36(3):507-14. doi: 10.1006/geno.1996.0496. Genomics. 1996. PMID: 8884274

3

Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus.

Peiffer-Schneider S, Schutte BC, Murray JC, Frees KL, Williamson K, Leysens NJ, Schwartz DA. Peiffer-Schneider S, et al. Among authors: schutte bc. Mamm Genome. 1997 Oct;8(10):785-6. doi: 10.1007/s003359900569. Mamm Genome. 1997. PMID: 9321479 No abstract available.

4

Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

Brennan TM, Landau D, Shalev H, Lamb F, Schutte BC, Walder RY, Mark AL, Carmi R, Sheffield VC. Brennan TM, et al. Among authors: schutte bc. Am J Hum Genet. 1998 Feb;62(2):355-61. doi: 10.1086/301708. Am J Hum Genet. 1998. PMID: 9463315 Free PMC article.

5

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC. Schutte BC, et al. Am J Med Genet. 1999 May 21;84(2):145-50. doi: 10.1002/(sici)1096-8628(19990521)84:2<145::aid-ajmg11>3.0.co;2-l. Am J Med Genet. 1999. PMID: 10323740

6

A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC. Schutte BC, et al. Genome Res. 2000 Jan;10(1):81-94. Genome Res. 2000. PMID: 10645953 Free PMC article.

7

Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.

Watanabe Y, Murray JC, Bjork BC, Bird CP, Chiang PW, Gregory SG, Kurnit DM, Schutte BC. Watanabe Y, et al. Among authors: schutte bc. Hum Mutat. 2001 Nov;18(5):422-34. doi: 10.1002/humu.1213. Hum Mutat. 2001. PMID: 11668635

8

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. Kondo S, et al. Among authors: schutte bc. Nat Genet. 2002 Oct;32(2):285-9. doi: 10.1038/ng985. Epub 2002 Sep 3. Nat Genet. 2002. PMID: 12219090 Free PMC article.

9

Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.

Kayano S, Kure S, Suzuki Y, Kanno K, Aoki Y, Kondo S, Schutte BC, Murray JC, Yamada A, Matsubara Y. Kayano S, et al. Among authors: schutte bc. J Hum Genet. 2003;48(12):622-628. doi: 10.1007/s10038-003-0089-0. Epub 2003 Nov 15. J Hum Genet. 2003. PMID: 14618417

10

Cleft palate: players, pathways, and pursuits.

Murray JC, Schutte BC. Murray JC, et al. Among authors: schutte bc. J Clin Invest. 2004 Jun;113(12):1676-8. doi: 10.1172/JCI22154. J Clin Invest. 2004. PMID: 15199400 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

112 results

Search Page

Filters