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Evidence for inheritance in patients with VACTERL association.
Solomon BD, Pineda-Alvarez DE, Raam MS, Cummings DA. Solomon BD, et al. Among authors: raam ms. Hum Genet. 2010 Jun;127(6):731-3. doi: 10.1007/s00439-010-0814-7. Epub 2010 Apr 6. Hum Genet. 2010. PMID: 20369369 Free PMC article.
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association.
Agochukwu NB, Pineda-Alvarez DE, Keaton AA, Warren-Mora N, Raam MS, Kamat A, Chandrasekharappa SC, Solomon BD. Agochukwu NB, et al. Among authors: raam ms. Eur J Med Genet. 2011 May-Jun;54(3):323-8. doi: 10.1016/j.ejmg.2011.01.007. Epub 2011 Feb 26. Eur J Med Genet. 2011. PMID: 21315191 Free PMC article.
Holoprosencephaly flashcards: A summary for the clinician.
Solomon BD, Pineda-Alvarez DE, Mercier S, Raam MS, Odent S, Muenke M. Solomon BD, et al. Among authors: raam ms. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):3-7. doi: 10.1002/ajmg.c.30245. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104594 Review.
De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene.
Solomon BD, Pineda-Alvarez DE, Hadley DW, Keaton AA, Agochukwu NB, Raam MS, Carlson-Donohoe HE, Kamat A, Chandrasekharappa SC. Solomon BD, et al. Among authors: raam ms. Birth Defects Res A Clin Mol Teratol. 2011 Sep;91(9):862-5. doi: 10.1002/bdra.20821. Epub 2011 May 23. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21608104 Free PMC article.
13 results