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Prenatal Diagnosis|February 4, 2021
Omphalocele-What should we tell the prospective parents?April D Adams, Samantha Stover, Martha W RacPrenatal Diagnosis|February 25, 2017
Targeted prenatal diagnosis of Pallister-Killian syndromeAnna Kucińska-Chahwan, Julia Bijok, Sylwia Dąbkowska, et al.Prenatal Diagnosis|March 16, 2017
Cryopreserved human umbilical cord versus biocellulose film for prenatal spina bifida repair in a physiologic rat modelSaul Snowise, Lovepreet Mann, Yisel Morales, et al.Prenatal Diagnosis|August 21, 2019
Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasmaOlle Ericsson, Tarja Ahola, Fredrik Dahl, et al.Prenatal Diagnosis|March 9, 2021
The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal settingRivka Sukenik-Halevy, Noa Ruhrman-Shahar, Naama Orenstein, et al.Prenatal Diagnosis|January 1, 1992
Future use and development of prenatal diagnosis. Consumers' attitudesB SjögrenPrenatal Diagnosis|January 1, 1992
Placental mosaicism in a case of 46,XY,-22,+t(22;22)(p11;q11) or i(22q) diagnosed at amniocentesisN B Spinner, Z Gibas, R Kline, et al.Prenatal Diagnosis|January 22, 2005
A novel L1CAM mutation with L1 spectrum disordersFatma Silan, Ismail Ozdemir, Willy LissensPrenatal Diagnosis|January 22, 2005
DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.Prenatal Diagnosis|January 22, 2005
Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locusE K Bijlsma, A C Knegt, C M Bilardo, et al.Pageof 695