Search Results - "Fetus"

PENGARUH PEMBERIAN ANTIBODI POLIKLONAL PMSG (Pregnant Mare Serum Gonadotropin) (Abpo PMSG) YANG BERASAL DARI KELINCI (Oryctolagus cuniculus) JANTAN TERHADAP JUMLAH FETUS MENCIT (Mus musculus) by indra rahmawati

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Correlação entre os parâmetros gasométricos e o grau de anemia em fetos de mães isoimunizadas Relationship between gasometry and the degree of anemia in fetus of maternal red cell by Juliana Moysés Barbosa Leite

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Detection of a heterozygous de novo pathogenic variant in the PTPN11 gene (c.1505 C > T, p.S502L) in a fetus associated with cystic hygroma and congenital heart defects by Chih-Ping Chen

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Emotional and cognitive experiences during the time of diagnosis and decision-making following a prenatal diagnosis: a qualitative study of males presented with congenital heart defect in the fetus carried by their pregnant partner by Tommy Carlsson, Elisabet Mattsson

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Avaliação crítica dos efeitos adversos do tratamento anti-retroviral no feto, recém-nascido e lactente Critical evaluation of the adverse effects of anti-retroviral treatment on the fetus, the newborn and the infant by Heloisa Helena de Sousa Marques

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Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion by Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Kevin Ko, Chen-Chi Lee, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

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Perbandingan Antara Perkiraan Umur KehamilanMelalui Hpmt (Hari Pertama Menstruasi Terakhir) DenganUltrasonografi Diameter Biparietal Fetus PadaTrimester Ketiga Di Rsud Dr.Moewardi Surakarta by Pradhana, Grata Vendy

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Indução do parto a termo com feto vivo com misoprostol vaginal: ensaio clínico aberto Induction of delivery at term with a live fetus with vaginal misoprostol: an open clinical assay by Zuleika Studart Sampaio

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A de novo heterozygous POU3F3 genotype for the p.(Q214*) variant in a fetus with transient isolated bilateral mild ventriculomegaly: a case report and review of the literature by Hongyun Zhang, Siyuan Linpeng, Yanling Teng, Can Peng, Desheng Liang, Desheng Liang, Zhuo Li, Lingqian Wu, Lingqian Wu

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Detection of tetrasomy 9p by chromosome microarray analysis and determination of maternal origin of the aberrant chromosome by quantitative fluorescent polymerase chain reaction in a second-trimester fetus with multiple anomalies on fetal ultrasound by Chih-Ping Chen

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Dopplerfluxometria de ducto venoso: identificação não invasiva da acidemia em fetos prematuros centralizados Ductus venosus velocimetry: noninvasive identification of fetal acidemia in preterm fetuses with brain sparing reflex by Renato Augusto Moreira de Sá, Hermógenes Chaves Netto, Laudelino Marques Lopes, Paulo Roberto Nassar de Carvalho, Ynesmara Coelho Cosmo

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Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study by Meiying Cai, Aixiang Lv, Wantong Zhao, Liangpu Xu, Na Lin, Hailong Huang

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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 by Chih-Ping Chen

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Prenatal diagnosis of a de novo 10p12.1p11.23 microdeletion encompassing the WAC gene in a fetus associated with bilateral hydronephrosis and right clubfoot on prenatal ultrasound by Chih-Ping Chen, Chen-Yu Chen, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Wayseen Wang

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Estudo do sonograma do ducto venoso em fetos com centralização hemodinâmica: avaliação de repercussões perinatais Study of ductus venosus in fetuses with brain sparing reflex: evaluation of perinatal outcomes by Paulo Roberto Nassar de Carvalho, Maria Elisabeth Lopes Moreira, Renato Augusto Moreira de Sá, Ynesmara Cosmos, Laudelino Marques Lopes

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Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia by Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Yu-Peng Liu, Cheng-Ran Peng, Yu-Ling Kuo, Peih-Shan Wu, Wen-Lin Chen, Wayseen Wang

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Transfusão intra-uterina em fetos afetados pela doença hemolítica perinatal grave: um estudo descritivo Intrauterine transfusion in fetuses affected by severe perinatal hemolytic disease: a descriptive study by Dorival Antônio Vitorello, Luiz Miguel Mitri Parente, Rodolfo João Ramos, Luís Flávio de Andrade Gonçalves, Cláudia Diniz Baumgarten, Jorge Abi Saab Neto

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Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3 by Shin-Wen Chen, Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Pei-Chen Wu, Yen-Ni Chen, Chen-Ju Lin, Wen-Ling Chen, Wayseen Wang

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Ventriculomegaly, Intrauterine Growth Restriction, and Congenital Heart Defects as Salient Prenatal Sonographic Findings of Miller-Dieker Lissencephaly Syndrome Associated With Monosomy 17p (17p13.2 → pter) in a Fetus by Chih-Ping Chen, Yu-Peng Liu, Shaun-Pei Lin, Ming Chen, Fuu-Jen Tsai, Yu-Ting Chen, Li-Feng Chen, Jonathan Kwei Hwang, Wayseen Wang

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Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus by Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wayseen Wang

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