Publications by authors named "Jacquelyn Roberson"

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High rates of "atypical" single nucleotide polymorphism-based noninvasive prenatal screening results among consanguineous Arab American patients: A single center retrospective study.
Mariam Ayyash, Sydney Daviskiba, Natalie Vriesen, Alyxandra Yaquinto, Jacquelyn Roberson

J Genet Couns· October 2023

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Recurrence Rate for Isolated Elevated Maternal Serum Alpha-Fetoprotein Levels and Pregnancy Outcomes.
Mariam Ayyash, Madhurima Keerthy, Jacquelyn Roberson, Majid Shaman

Genet Test Mol Biomarkers· September 2022

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Biallelic Variants in Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy.
Kuntal Sen, Shagun Kaur, David W Stockton, Mary Nyhuis, Jacquelyn Roberson

AJP Rep· January 2021

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A novel SERPINA1 mutation causing serum alpha(1)-antitrypsin deficiency.
Darren N Saunders, Elizabeth A Tindall, Robert F Shearer, Jacquelyn Roberson, Amy Decker

PLoS One· June 2013

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False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
Sainan Wei, Victoria Mok Siu, Amy Decker, Mary-Helen Quigg, Jacquelyn Roberson

Prenat Diagn· November 2007

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Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
David B Everman, Chad T Morgan, Robert Lyle, Mary E Laughridge, Michael J Bamshad, Jacquelyn Roberson

Am J Med Genet A· July 2006

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Regarding trisomy 18.
Robert Roger Lebel, Jacquelyn Roberson, Daniel L Van Dyke

Am J Med Genet A· May 2006

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