Search Results - "Fetus"

Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene by Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Yi-Ning Su, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang

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Novel characterization of CASK variant c.1963 A>G (p.Asn655Asp) through whole-exome sequencing in a monochorionic diamniotic twin fetus with significant brain anomalies: A case report by Nathan A. Keller, Luis A. Bracero, Insaf Kouba, Abigail Steinberg, Jolene Muscat, David Bergman

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Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Observed to expected lung area to head circumference ratio (O/E LHR) in fetuses with congenital anomalies of the kidney and urinary tract (CAKUT): assessment and evaluation as predictive factor for acute postnatal outcome-a single center study by M. Sourouni, M. Sourouni, L. Haisch, K. Oelmeier, M. Möllers, D. Willy, K. Sondern, H. Köster, J. Steinhard, J. Sandkötter, W. Klockenbusch, R. Schmitz, J. Potratz

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Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound by Chih-Ping Chen, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang

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Maternal serum soluble fms-like tyrosine kinase-1-to-placental growth factor ratio distinguishes growth-restricted from non-growth-restricted small-for-gestational-age fetusesAJOG Global Reports at a Glance by Prithi Rajiv, MD, Thomas Cade, MD, Jennifer Dean, MD, Gabriel Davis Jones, MD, Shaun P. Brennecke, MD, PhD

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Efeitos da administração diária da associação estavudina/nelfinavir sobre os fetos e placentas da rata albina Effects of daily administration of a stavudine/nelfinavir association on the fetuses and placentas of female albino rats by Gisela Maria Vieira Rodrigues de Carvalho, Mary Uchiyama Nakamura, Ricardo Santos Simões, Eliana Maria Restum Antonio, Adriana Wagngner, Tereza Maria Pereira Fontes, Luiz Kulay Júnior

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Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcome by Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang

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Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome by Wen-Xu Yang, Hong Pan, Song-Tao Wang, Lin Li, Hai-Rong Wu, Yu Qi

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Correlação entre medidas ultra-sonográficas do coração e o deficit de hemoglobina em fetos de gestantes aloimunizadas Correlation between echographic cardiac measurements and hemoglobin deficit in fetus of red cell alloimmunized pregnancies by Marília Zicker Hanan, Antônio Carlos Vieira Cabral, Alamanda Kfoury Pereira, Henrique Vitor Leite, Zilma Nogueira Reis

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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 by Luiz Camano, Antonio Fernandes Moron, Luciano Marcondes Machado Nardozza, David Baptista da Silva Pares, Paulo Alexandre Chinen

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Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly by Pi-Lin Sung, Chia-Ming Chang, Chih-Yao Chen, Peng-Hui Wang, Kuan-Chong Chao, Kuo-Chang Wen, Yung-Yung Cheng, Yueh-Chun Li, Chyi-Chyang Lin

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Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound by Chih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang

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Fatores associados à indução do parto em gestantes com óbito fetal após a 20ª semana Factors associated with induced delivery in pregnant women with a dead fetus after the 20th week of gestation by Ânderson Gonçalves Sampaio, Alex Sandro Rolland Souza, Carlos Noronha Neto

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Incidental detection of a de novo 16p13.3 microdeletion encompassing PKD1 and a familial Yq11.223 microdeletion encompassing DAZ1 in a fetus with encephalocele on prenatal ultrasound and amniotic band syndrome by Chih-Ping Chen

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Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs by Chih-Ping Chen, Shih-Shien Weng, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Oclusão traqueal para fetos com hérnia diafragmática esquerda grave isolada: um estudo experimental controlado não randomizado Tracheal occlusion for fetuses with severe isolated left-sided diaphragmatic hernia: a nonrandomized controlled experimental study by Cleisson Fábio Andrioli Peralta, Lourenço Sbragia, João Renato Bennini, Ricardo Carvalho Cavalli, Monique Sampaio Rousselet, Ricardo Barini

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Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound by Chih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Dai-Dyi Town, Li-Feng Chen, Wayseen Wang

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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 by Chih-Ping Chen

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Análise morfológica dos fígados e rins no binômio materno-fetal após tratamento de ratas prenhes com Ritonavir durante toda a prenhez Morphological analysis of liver and kidneys of pregnant rats and their fetuses upon chronic Ritonavir administration by Adelino Moreira de Carvalho, Ricardo Santos Simões, Fábio Hideo Martins Oliveira, Manuel de Jesus Simões, Ricardo Martins Oliveira-Filho, Mary Uchiyama Nakamura, Luiz Kulay Júnior

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