Search Results - "Simi, Eve"

De novo mosaic and partial monosomy of chromosome 21 in a case with superior vena cava duplication by Azad, Abul Kalam, Yanakakis, Lindsay, Issleb, Samantha, Turina, Jessica, Drabik, Kelli, Bonner, Christina, Simi, Eve, Wagner, Andrew, Fiddler, Morry, Naeem, Rizwan

“…Full or partial monosomy of chromosome (chr) 21 is a very rare abnormal cytogenetic finding. It is characterized by variable sizes and deletion breakpoints on…”
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Exploring prenatal genetic counselors' perceptions of abortion laws in restrictive states by Koenig, Shelby, Simi, Eve, Goldenberg, Aaron, Magasi, Susan, Wicklund, Catherine

“…In many states, abortion laws are becoming increasingly restrictive. Prenatal genetic counselors often see patients after the diagnosis of a fetal abnormality…”
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Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States by Jayaraman, Susheela, Koenig, Shelby, Fiddler, Morry, Simi, Eve, Goldenberg, Aaron, Magasi, Susan, Wicklund, Catherine

“…Genetic counselors have an important role in offering and appropriate coordinating abortion services for patients identified with a fetal abnormality. Few…”
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Clinical implementation of noninvasive prenatal testing among maternal fetal medicine specialists by Haymon, Lori, Simi, Eve, Moyer, Kelly, Aufox, Sharon, Ouyang, David W.

“…ABSTRACT Objective To assess the clinical implementation of non‐invasive prenatal testing (NIPT) among maternal‐fetal medicine (MFM) specialists. Method…”
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Clinical implementation of noninvasive prenatal testing among maternal fetal medicine specialists: Clinical Implementation of NIPT among MFMs by Haymon, Lori, Simi, Eve, Moyer, Kelly, Aufox, Sharon, Ouyang, David W.

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De novo mosaic and partial monosomy of chromosome 21 in a case with superior vena cava duplication by Azad, Abul Kalam, Yanakakis, Lindsay, Issleb, Samantha, Turina, Jessica, Drabik, Kelli, Bonner, Christina, Simi, Eve, Wagner, Andrew, Fiddler, Morry, Naeem, Rizwan

“…BACKGROUNDFull or partial monosomy of chromosome (chr) 21 is a very rare abnormal cytogenetic finding. It is characterized by variable sizes and deletion…”
Get full text