Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis

Por Westerfield, Lauren, Darilek, Sandra, van den Veyver, Ignatia B.
Publicado no J Clin Med (2014)

Genetic counseling for men with recurrent pregnancy loss or recurrent implantation failure due to abnormal sperm chromosomal aneuploidy

Por Kohn, Taylor P., Kohn, Jaden R., Darilek, Sandra, Ramasamy, Ranjith, Lipshultz, Larry
Publicado no J Assist Reprod Genet (2016)

Obstetrician and Gynecologist Utilization of the Noninvasive Prenatal Testing Expanded Option

Por Mayes, Sarah, Hashmi, Syed, Turrentine, Mark A., Darilek, Sandra, Friel, Lara A., Czerwinski, Jennifer
Publicado no AJP Rep (2015)

Infrequency of Two Deletion Mutations at the DFNB1 Locus in Patients and Controls

Por Tang, Hsiao-Yuan, Basehore, Monica J., Blakey, Gregory L., Darilek, Sandra, Oghalai, John S., Roa, Benjamin B., Fang, Ping, Alford, Raye Lynn
Publicado em 2008

DNA Sequence Analysis of GJB2, Encoding Connexin 26: Observations From a Population of Hearing Impaired Cases and Variable Carrier Rates, Complex Genotypes, and Ethnic Stratificati...

Por Tang, Hsiao-Yuan, Fang, Ping, Ward, Patricia A., Schmitt, Eric, Darilek, Sandra, Manolidis, Spiros, Oghalai, John S., Roa, Benjamin B., Alford, Raye Lynn
Publicado em 2006

DNA sequence analysis and genotype–phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy

Por Tang, Hsiao-Yuan, Fang, Ping, Lin, Jerry W, Darilek, Sandra, Osborne, Brooke T, Haymond, Jo Ann, Manolidis, Spiros, Roa, Benjamin B, Oghalai, John S, Alford, Raye L
Publicado no BMJ Open (2015)

The ethics of conducting molecular autopsies in cases of sudden death in the young

Por McGuire, Amy L., Moore, Quianta, Majumder, Mary, Walkiewicz, Magdalena, Eng, Christine M., Belmont, John W., Nassef, Salma, Darilek, Sandra, Rutherford, Katie, Pereira, Stacey, Scherer, Steven E., Sutton, V. Reid, Wolf, Dwayne, Gibbs, Richard A., Kahn, Roger, Sanchez, Luis A.
Publicado no Genome Res (2016)

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases()

Por Van den Veyver, Ignatia B., Patel, Ankita, Shaw, Chad A., Pursley, Amber N., Kang, Sung-Hae L., Simovich, Marcia J., Ward, Patricia A., Darilek, Sandra, Johnson, Anthony, Neill, Sarah E., Bi, Weimin, White, Lisa D., Eng, Christine M., Lupski, James R., Cheung, Sau Wai, Beaudet, Arthur L.
Publicado em 2009