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1. Sanders' structural fetal abnormalities
by Hill, Lyndon, editor and Hogge, W. Allen, editor and Wilkins, Isabelle A., editor and Cohlan, Barbara, editor
2017, Third edition., ISBN 9781259641374, xi, 644 pages
Fetus | Ultrasonic imaging | Abnormalities
Book
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2. Full Text A practical guide to fetal echocardiography
: normal and abnormal hearts
by Abuhamad, Alfred, author and Chaoui, Rabih, author
2016, Third edition., ISBN 1451176058, 944
Heart Defects, Congenital | Ultrasonography, Prenatal | ultrasonography | methods | Fetal Heart | Fetal heart | Ultrasonic imaging
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3. Full Text Diagnosis of fetal non‐chromosomal abnormalities on routine ultrasound examination at 11–13 weeks' gestation
by Syngelaki, A and Hammami, A and Bower, S and Zidere, V and Akolekar, R and Nicolaides, K. H
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2019, Volume 54, Issue 4, pp. 468 - 476
ultrasound examination | prenatal diagnosis | fetal abnormalities | first‐trimester screening | Acoustics | Life Sciences & Biomedicine | Technology | Radiology, Nuclear Medicine & Medical Imaging | Obstetrics & Gynecology | Science & Technology | Fetus - abnormalities | Pregnancy Trimester, Second | Congenital Abnormalities - epidemiology | Fetus - diagnostic imaging | Humans | Nuchal Translucency Measurement - methods | Congenital Abnormalities - diagnostic imaging | Gestational Age | Pregnancy Trimester, First | Pregnancy Trimester, Third | Adult | Female | Pregnancy - ethnology | Ultrasonography, Prenatal - methods | Retrospective Studies | Fetus - anatomy & histology | Prenatal Care - standards | Index Medicus
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4. Fetal diagnosis and therapy
and International Fetal Medicine and Surgery SocietyInternational Society of the Fetus as a Patient
Fetal diagnosis and therapy, ISSN 1015-3837, 1991
Fetus | Diagnosis | Perinatology | Diseases
Journal
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5. Full Text Prenatal craniofacial abnormalities: from ultrasonography to three‐dimensional printed models
by Nicot, R and Druelle, C and Hurteloup, E and Levaillant, J.‐M
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 12/2019, Volume 54, Issue 6, pp. 835 - 836
Acoustics | Life Sciences & Biomedicine | Technology | Radiology, Nuclear Medicine & Medical Imaging | Obstetrics & Gynecology | Science & Technology | Fetus - abnormalities | Craniofacial Dysostosis - pathology | Fetus - diagnostic imaging | Face - abnormalities | Humans | Craniofacial Dysostosis - diagnostic imaging | Gestational Age | Craniofacial Abnormalities - diagnostic imaging | Pregnancy | Printing, Three-Dimensional - instrumentation | Cleft Lip - pathology | Imaging, Three-Dimensional - instrumentation | Cleft Lip - diagnostic imaging | Craniofacial Abnormalities - pathology | Face - diagnostic imaging | Female | Ultrasonography, Prenatal - methods | Ultrasonography, Prenatal - standards | Preoperative Period | Ultrasound | Abnormalities | Index Medicus
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6. Full Text Zika Virus Infection with Prolonged Maternal Viremia and Fetal Brain Abnormalities
by Driggers, Rita W and Ho, Cheng-Ying and Korhonen, Essi M and Kuivanen, Suvi and Jääskeläinen, Anne J and Smura, Teemu and Rosenberg, Avi and Hill, D. Ashley and DeBiasi, Roberta L and Vezina, Gilbert and Timofeev, Julia and Rodriguez, Fausto J and Levanov, Lev and Razak, Jennifer and Iyengar, Preetha and Hennenfent, Andrew and Kennedy, Richard and Lanciotti, Robert and du Plessis, Adre and Vapalahti, Olli
The New England journal of medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 22, pp. 2142 - 2151
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Fetus - abnormalities | Brain - embryology | Pregnancy Complications, Infectious - virology | Viremia | Humans | Brain - virology | Brain - abnormalities | Zika Virus - isolation & purification | Microcephaly - virology | Pregnancy | Magnetic Resonance Imaging | Zika Virus Infection - epidemiology | Disease Outbreaks | Ultrasonography, Prenatal | Brain - pathology | Zika Virus Infection - complications | Adult | Female | Practice guidelines (Medicine) | Complications and side effects | Brain | Analysis | Abnormalities | Neuroimaging | Fetuses | Cortex | Outbreaks | Birth defects | Zika virus | Gestation | Ribonucleic acid--RNA | Microencephaly | Magnetic resonance imaging | Maternal & child health | Autopsy | Ultrasonography | Viral infections | Index Medicus | Abridged Index Medicus
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7. Full Text Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis
by Boissel, Sarah and Fallet-Bianco, Catherine and Chitayat, David and Kremer, Valérie and Nassif, Christina and Rypens, Françoise and Delrue, Marie-Ange and Dal Soglio, Dorothée and Oligny, Luc L and Patey, Natalie and Flori, Elisabeth and Cloutier, Mireille and Dyment, David and Campeau, Philippe and Karalis, Aspasia and Nizard, Sonia and Fraser, William D and Audibert, François and Lemyre, Emmanuelle and Rouleau, Guy A and Hamdan, Fadi F and Kibar, Zoha and Michaud, Jacques L
Genetics in medicine, ISSN 1098-3600, 07/2018, Volume 20, Issue 7, pp. 745 - 753
fetal anomalies | GREB1L | exome sequencing | birth defects | de novo mutations | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Abnormalities, Multiple - pathology | Fetus - abnormalities | Limb Deformities, Congenital - genetics | Genomics | Humans | Fetus - pathology | Male | Stillbirth - genetics | Whole Exome Sequencing - methods | Kidney Diseases - genetics | Spine - abnormalities | Heart Defects, Congenital - genetics | Congenital Abnormalities - genetics | Adult | Female | Hydrocephalus - genetics | Neoplasm Proteins - genetics | Abnormalities, Multiple - genetics | Trachea - abnormalities | Kidney Diseases - congenital | Genotype | Esophagus - abnormalities | Anal Canal - abnormalities | Pregnancy | Phenotype | Kidney - abnormalities | Tracheoesophageal Fistula - genetics | Family | Mutation | Prenatal Diagnosis - methods | Urogenital Abnormalities - genetics | Index Medicus
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8. Scientific frontiers in developmental toxicology and risk assessment
and National Research Council (U.S.) and National Research Council (U.S.). Board on Environmental Studies and Toxicology and National Research Council (U.S.). Committee on Developmental ToxicologyNational Research Council (U.S.). Commission on Life Science
2000, ISBN 0309070864, xviii, 327
Health risk assessment | Developmental toxicology
Book
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9. Full Text DNA methylation abnormalities in congenital heart disease
by Serra-Juhé, Clara and Cuscó, Ivon and Homs, Aïda and Flores, Raquel and Torán, Núria and Pérez-Jurado, Luis A
Epigenetics, ISSN 1559-2294, 02/2015, Volume 10, Issue 2, pp. 167 - 177
congenital heart disease | DNA methylation | epimutation | Down syndrome | heart malformation | Epimutation | Congenital heart disease | Heart malformation | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genome-Wide Association Study | Humans | Middle Aged | Fetus - metabolism | Heart Defects, Congenital - pathology | Male | DNA - metabolism | DNA - blood | Pregnancy | Young Adult | Heart Defects, Congenital - genetics | DNA Methylation | Myocardium - metabolism | Aged, 80 and over | Adult | Female | Aged | Index Medicus | Malalties coronàries | ADN
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10. Full Text Amniotic Fluid Abnormalities
by Harman, Christopher R., MD
Seminars in perinatology, ISSN 0146-0005, 2008, Volume 32, Issue 4, pp. 288 - 294
Neonatal and Perinatal Medicine | maximum vertical pocket | amnioreduction | perinatal outcome | amnioinfusion | amniotic fluid | Pediatrics | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Pregnancy | Fetus - abnormalities | Fetal Diseases - diagnosis | Oligohydramnios | Ultrasonography, Prenatal | Humans | Prenatal Diagnosis | Female | Amniotic Fluid - physiology | Polyhydramnios | Index Medicus
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11. Full Text Associated anomalies in cases with esophageal atresia
by Stoll, Claude and Alembik, Yves and Dott, Beatrice and Roth, Marie‐Paule
American journal of medical genetics. Part A, ISSN 1552-4825, 08/2017, Volume 173, Issue 8, pp. 2139 - 2157
tracheooesophageal fistula | congenital anomalies | congenital malformations | esophageal atresia | VACTERL association | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Chromosome Disorders - epidemiology | Limb Deformities, Congenital - genetics | Congenital Abnormalities - epidemiology | Esophageal Atresia - epidemiology | Humans | Congenital Abnormalities - physiopathology | Stillbirth | Limb Deformities, Congenital - physiopathology | Male | Spine - abnormalities | Esophagus - physiopathology | Heart Defects, Congenital - genetics | Congenital Abnormalities - genetics | Anal Canal - physiopathology | Abnormalities, Multiple - epidemiology | Female | Esophageal Atresia - genetics | Trachea - physiopathology | Esophageal Atresia - complications | Chromosome Disorders - physiopathology | Abnormalities, Multiple - genetics | Kidney - physiopathology | Trachea - abnormalities | Esophageal Atresia - physiopathology | Chromosome Disorders - complications | Spine - physiopathology | Fetus - physiopathology | Esophagus - abnormalities | Abnormalities, Multiple - physiopathology | Anal Canal - abnormalities | Pregnancy | Heart Defects, Congenital - complications | Kidney - abnormalities | Limb Deformities, Congenital - epidemiology | Chromosome Aberrations | Heart Defects, Congenital - epidemiology | Limb Deformities, Congenital - complications | Heart Defects, Congenital - physiopathology | Chromosome Disorders - genetics | Development and progression | Birth defects | Genetic disorders | Etiology | Congenital defects | Hernias | Fetuses | CHARGE syndrome | Infants | Sudden infant death syndrome--SIDS | Esophagus | Index Medicus
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12. Full Text Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases
by Pasquier, Laurent and Pasquier, Laurent and Marcorelles, Pascale and Marcorelles, Pascale and Loget, Philippe and Loget, Philippe and Pelluard, Fanny and Pelluard, Fanny and Carles, Dominique and Carles, Dominique and Perez, Marie-Josée and Perez, Marie-Josée and Bendavid, Claude and Bendavid, Claude and de La Rochebrochard, Céline and de La Rochebrochard, Céline and Ferry, Mathilde and Ferry, Mathilde and David, Véronique and David, Véronique and Odent, Sylvie and Odent, Sylvie and Laquerrière, Annie and Laquerrière, Annie
Acta neuropathologica, ISSN 0001-6322, 2/2009, Volume 117, Issue 2, pp. 185 - 200
Pathology | Neurosciences | Medicine & Public Health | Rhombencephalosynapsis | Aqueductal atresia | Hydrocephalus | Neural tube defects | VACTERL-H syndrome | Holoprosencephaly | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Abnormalities, Multiple - pathology | Cerebral Ventricles - pathology | Immunohistochemistry | Fetus - abnormalities | Brain - embryology | Humans | Craniofacial Abnormalities - embryology | Hydrocephalus - pathology | Male | Brain - abnormalities | Cerebellum - abnormalities | Abnormalities, Multiple - embryology | Syndrome | Cerebellum - pathology | Cerebellum - embryology | Hydrocephalus - embryology | Cerebral Ventricles - abnormalities | Brain - pathology | Craniofacial Abnormalities - pathology | Female | Cerebral Ventricles - embryology | Index Medicus | Cerebellum | Brain | Neurons and Cognition | Abnormalities, Multiple | Life Sciences | Cerebral Ventricles | Fetus | Genetics | Craniofacial Abnormalities | Development Biology
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