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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2002 | 2 |
2004 | 2 |
2007 | 1 |
2009 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
Atypical X-chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomy.
Am J Med Genet A. 2009 Mar;149A(3):408-14. doi: 10.1002/ajmg.a.32699.
Am J Med Genet A. 2009.
PMID: 19215059
Free PMC article.
X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.
Kimani JW, Shi M, Daack-Hirsch S, Christensen K, Moretti-Ferreira D, Marazita ML, Field LL, Canady JW, Murray JC.
Kimani JW, et al.
Am J Med Genet A. 2007 Dec 15;143A(24):3267-72. doi: 10.1002/ajmg.a.32098.
Am J Med Genet A. 2007.
PMID: 18000982
Free PMC article.
Item in Clipboard
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, Ray A, Moreno L, Valencia C, Neiswanger K, Wyszynski DF, Bailey-Wilson JE, Albacha-Hejazi H, Beaty TH, McIntosh I, Hetmanski JB, Tunçbilek G, Edwards M, Harkin L, Scott R, Roddick LG.
Marazita ML, et al.
Am J Hum Genet. 2004 Aug;75(2):161-73. doi: 10.1086/422475. Epub 2004 Jun 4.
Am J Hum Genet. 2004.
PMID: 15185170
Free PMC article.
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TBX22 mutations are a frequent cause of cleft palate.
Marçano AC, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P.
Marçano AC, et al.
J Med Genet. 2004 Jan;41(1):68-74. doi: 10.1136/jmg.2003.010868.
J Med Genet. 2004.
PMID: 14729838
Free PMC article.
No abstract available.
Item in Clipboard
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.
Nat Genet. 2002 Oct;32(2):285-9. doi: 10.1038/ng985. Epub 2002 Sep 3.
Nat Genet. 2002.
PMID: 12219090
Free PMC article.
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The role of MSX1 in human tooth agenesis.
Lidral AC, Reising BC.
Lidral AC, et al.
J Dent Res. 2002 Apr;81(4):274-8. doi: 10.1177/154405910208100410.
J Dent Res. 2002.
PMID: 12097313
Free PMC article.
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Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.
Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW.
Erickson RP, et al.
J Med Genet. 2001 Nov;38(11):761-6. doi: 10.1136/jmg.38.11.761.
J Med Genet. 2001.
PMID: 11694548
Free PMC article.
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