Resultados de búsqueda - "nuchal translucency"

Prenatal diagnosis of Smith-Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects por Ting-Ying Lei, Ru Li, Fang Fu, Jun-Hui Wan, Yong-Ling Zhang, Xiang-Yi Jing, Can Liao

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Late onset of large benign ductus arteriosus aneurysm presented with increased nuchal translucency and cystic hygroma at first trimester Down syndrome screening por Horng-Der Tsai, Kuanting Chen, Meng-Luen Lee, Cheng-Han Lee, Tze-Ho Chen, Wen-Hsiang Lin, Ming Chen

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Intertwin nuchal translucency difference predicts the chance of co-twin death after fetal reduction in dichorionic triplet pregnancies: a retrospective analysis study por Shuting Xia, Kaniok You, Minhuan Lin, Linhuan Huang, Zhiming He, Xuan Huang, Yanmin Luo

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The Association between Intertwin Difference in First Trimester Crown-Rump Length, Nuchal Translucency, and Birth Weight Discordance in Twin Pregnancies: A Retrospective Cohort Study por Zachary Michael Ferraro, Tinghua Zhang, Felipe Moretti, Karen Fung-

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Relationship between extreme values of first trimester maternal pregnancy associated plasma Protein-A, free-β-human chorionic gonadotropin, nuchal translucency and adverse pregnancy outcomes por Simten Genc, Hale Ozer, Cagdas Nurettin Emeklioglu, Basak Cingillioglu, Orhan Sahin, Erhan Akturk, Hicran Acar Sirinoglu, Nilgun Basaran, Veli Mihmanli

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Corrigendum to <'Real-time quality control of nuchal translucency measurements using the exponentially weighted moving average chart' [Taiwanese Journal of Obstetrics & Gynecology 60 (2021) 84-89] por Martin Hynek, Jana Zvárová, Dagmar Smetanová, David Stejskal, Jan Kalina

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Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound por Chih-Ping Chen

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Rapid detection of paternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction analysis in a fetus associated with increased nuchal translucency thickness and in a pregnancy without an advanced maternal age por Chih-Ping Chen

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Partial monosomy 13q (13q21.32→qter) and partial trisomy 8p (8p12→pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization por Chih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, Ming-Huei Lin, Pei-Chen Wu, Schu-Rern Chern, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang

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Avaliação do desfecho dos conceptos com risco aumentado de ocorrência de anomalias cromossômicas calculado pela medida da translucência nucal Outcome of fetuses with increased risk of chromosomal anomalies, based on nuchal translucency measurement por Luiz Camano, Antonio Fernandes Moron, Luciano Marcondes Machado Nardozza, David Baptista da Silva Pares, Paulo Alexandre Chinen

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Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester por Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Chin-Yuan Hsu, Yi-Yung Chen, Jun-Wei Su, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang

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Spontaneous resolution of septated cystic hygroma with a severely increased nuchal translucency thickness of 5.8 mm detected in the first-trimester in a pregnancy with no abnormalities in chromosomal, microarray and whole exome sequencing analyses and a favorable fetal outcome por Chih-Ping Chen, Shin-Wen Chen, Fang-Tzu Wu, Yen-Ting Pan, Wayseen Wang

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Aumento de la translucencia nucal y flujo reverso del ductus venoso en cardiopatía congénita: Reporte de un caso en Caracas, Venezuela Increased foetal nuchal translucency and reverse flow of the ductus venosus in congenital cardiopathy por Cristian Sosa, Libardo Gómez, Carlos Bermúdez, Juan Pérez-Wulff

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Rapid confirmation of maternal origin of trisomy 21 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency, abnormal first-trimester maternal serum screening result and positive non-invasive prenatal testing for trisomy 21 por Chih-Ping Chen

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Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results por Chih-Ping Chen, Jui-Der Liou, Kok-Min Seow, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Li-Feng Chen, Wayseen Wang

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Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency por Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Li-Feng Chen, Wayseen Wang

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Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result por Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

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Rapid diagnosis of maternal origin of de novo fetal Robertsonian translocation down syndrome of 46,XY,der(13;21)(q10;q10),+21 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with increased nuchal translucency and an abnormal result of first-trimester maternal serum screening por Chih-Ping Chen

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Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome por Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang

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Early Prenatal Sonographic Diagnosis of Lethal Arthrogryposis Multiplex Congenita: A Case Presentation por Kazım Gezginç, Rengin Karataylı, Fatma Yazıcı, Tuba Tursun, Ali Acar

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