Torthaí cuardaigh - Stal, Samuel
- 1 - 11 toradh as 11 á dtaispeáint
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1
Rhinoplasty in the Hispanic Patient de réir Higuera, Stephen, Hatef, Daniel A., Stal, Samuel
Foilsithe / Cruthaithe 2009Téacs -
2
Evaluation and Reduction of Nasal Trauma de réir Kelley, Brian P., Downey, Cara R., Stal, Samuel
Foilsithe / Cruthaithe 2010Téacs -
3
Cleft Nasal Deformity and Rhinoplasty de réir Kaufman, Yoav, Buchanan, Edward P., Wolfswinkel, Erik M., Weathers, William M., Stal, Samuel
Foilsithe / Cruthaithe 2012Téacs -
4
Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate de réir Blanton, Susan H., Burt, Amber, Stal, Samuel, Mulliken, John B., Garcia, Elizabeth, Hecht, Jacqueline T.
Foilsithe / Cruthaithe 2010Téacs -
5
Ethnic heterogeneity of IRF6 AP-2α binding site promoter SNP association with nonsyndromic cleft lip and palate de réir Blanton, Susan H., Burt, Amber, Garcia, Elizabeth, Mulliken, John B., Stal, Samuel, Hecht, Jacqueline T.
Foilsithe / Cruthaithe 2010Téacs -
6
Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate de réir Chiquet, Brett T., Blanton, Susan H., Burt, Amber, Ma, Deqiong, Stal, Samuel, Mulliken, John B., Hecht, Jacqueline T.
Foilsithe / Cruthaithe 2008Téacs -
7
Nonsyndromic cleft lip and palate: CRISPLD Genes and the Folate Gene Pathway Connection de réir Chiquet, Brett T., Henry, Robin, Burt, Amber, Mulliken, John B., Stal, Samuel, Blanton, Susan H., Hecht, Jacqueline T.
Foilsithe / Cruthaithe 2010Téacs -
8
The Folate Pathway and Nonsyndromic Cleft Lip and Palate de réir Blanton, Susan H., Henry, Robin R., Yuan, Quiping, Mulliken, John B., Stal, Samuel, Finnell, Richard H., Hecht, Jacqueline T.
Foilsithe / Cruthaithe 2010Téacs -
9
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate de réir Chiquet, Brett T, Hashmi, Syed S, Henry, Robin, Burt, Amber, Mulliken, John B, Stal, Samuel, Bray, Molly, Blanton, Susan H, Hecht, Jacqueline T
Foilsithe / Cruthaithe 2009Téacs -
10
CRISPLD2: a novel NSCLP candidate gene de réir Chiquet, Brett T., Lidral, Andrew C., Stal, Samuel, Mulliken, John B., Moreno, Lina M., Arco-Burgos, Mauricio, Valencia-Ramirez, Consuelo, Blanton, Susan H., Hecht, Jacqueline T.
Foilsithe / Cruthaithe 2007Téacs -
11
Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome de réir Heilstedt, Heidi A., Ballif, Blake C., Howard, Leslie A., Lewis, Richard A., Stal, Samuel, Kashork, Catherine D., Bacino, Carlos A., Shapira, Stuart K., Shaffer, Lisa G.
Foilsithe / Cruthaithe 2003Téacs