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American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2016, Volume 214, Issue 1, pp. S345 - S345
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.ajog.2015.10.694 Byline: Trissa McClatchey, Erica Lay, Melissa... 
Obstetrics and Gynecology | Genetic counseling | Medical genetics
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 01/2016, Volume 214, Issue 1, p. S309
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.ajog.2015.10.620 Byline: Jaclyn B. Murry, David Engler, Rajesh... 
Genetic research | Fluoxetine
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2016, Volume 214, Issue 1, pp. S309 - S309
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 03/2019, Volume 39, Issue 4, pp. 319 - 323
What's already known? Pan‐ethnic expanded carrier screening (ECS) can now be offered to all patients for a wide number of diseases to determine one's carrier... 
STATEMENT | OBSTETRICIANS | GYNECOLOGISTS | ATTITUDES | GENETICS & HEREDITY | OBSTETRICS & GYNECOLOGY | Pregnancy | Genetic counseling | Pregnant women | Medical genetics | Medical records | Women, Jewish | Obstetrics | Psychiatric services | Screening | Demographics | Prenatal development | Minority & ethnic groups | Genetic screening | Gestational age
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 01/2016, Volume 214, Issue 1, pp. S309 - S309
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2017, Volume 12, Issue 1, pp. e0170127 - e0170127
Offspring of murine dams chronically fed a protein-restricted diet have an increased risk for metabolic and neurobehavioral disorders. Previously we showed... 
LATER LIFE | TRYPTOPHAN DEPLETION | ADULT RATS | NEURON NUMBERS | MULTIDISCIPLINARY SCIENCES | INBRED STRAINS | PRENATAL MALNUTRITION | GENE-EXPRESSION | PHYSICAL GROWTH | HIPPOCAMPAL-FORMATION | OBSESSIVE-COMPULSIVE DISORDER | Gene Expression | Maternal Nutritional Physiological Phenomena | Hypothalamus - physiology | Mice, Inbred C57BL | Circadian Rhythm - genetics | Male | Circadian Rhythm - physiology | Behavior, Animal | Animals | Energy Metabolism | Diet, Protein-Restricted - adverse effects | Liver - physiology | Female | Sleep - physiology | Adipose Tissue | Anxiety - etiology | Enzymes | Sleep | Diet | Body weight | Physiological aspects | Mice | Gene expression | Breastfeeding & lactation | Night | Body fat | Liver | Memory | Mental depression | Assaying | Proteins | Learning | Period 1 protein | Physiology | Anxiety | Food composition | Behavior | Conditioning | Low protein diet | Circadian rhythms | Dams | Gynecology | Exposure | Marble | Fear conditioning | Serum levels | Nutrition research | Offspring | Hospitals | Food intake | Adults | Metabolic disorders | Neurosciences | Weaning | Hypothalamus | Body composition | Mating | Energy | Body composition (biology) | Rodents | Zeitgeber | Casualties | Malnutrition | Open-field behavior | Muscles | Energy expenditure | Exploration | Rhythm | Circadian rhythm | Obstetrics | Medicine | Fear | Progeny | Anxieties | Laboratory animals | Index Medicus
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 12/2017, Volume 217, Issue 6, pp. 691.e1 - 691.e6
Since its debut in 2011, cell-free fetal DNA screening has undergone rapid expansion with respect to both utilization and coverage. However, conclusive data... 
amniocentesis | trisomy 13 | trisomy 21 | 47,XXY | noninvasive prenatal testing | noninvasive prenatal screening | 47,XXX | 47,XYY | cell-free DNA | NIPT | prenatal diagnosis | microdeletion syndrome | trisomy 18 | CHROMOSOMAL MICROARRAY | TRISOMIES 21 | FREE DNA | RISK | CLINICAL-EXPERIENCE | OBSTETRICS & GYNECOLOGY | FETAL ANEUPLOIDIES | Chromosome Disorders - blood | Predictive Value of Tests | Turner Syndrome - blood | Cri-du-Chat Syndrome - diagnosis | Humans | Angelman Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - genetics | Turner Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - blood | Trisomy 18 Syndrome - diagnosis | Cri-du-Chat Syndrome - genetics | Klinefelter Syndrome - blood | Klinefelter Syndrome - genetics | Sex Chromosome Aberrations | Microarray Analysis | Karyotyping | Down Syndrome - blood | Angelman Syndrome - genetics | Chorionic Villi Sampling | Chromosome Disorders - diagnosis | Prader-Willi Syndrome - genetics | Female | Down Syndrome - diagnosis | Amniocentesis | Prader-Willi Syndrome - diagnosis | Trisomy 13 Syndrome - genetics | Chromosomes, Human, X - genetics | Prader-Willi Syndrome - blood | Prenatal Diagnosis | In Situ Hybridization, Fluorescence | Cri-du-Chat Syndrome - blood | Pregnancy | Trisomy 18 Syndrome - blood | Sex Chromosome Disorders of Sex Development - diagnosis | Trisomy - diagnosis | Trisomy - genetics | Trisomy 13 Syndrome - blood | Cell-Free Nucleic Acids - blood | Trisomy 18 Syndrome - genetics | Down Syndrome - genetics | Klinefelter Syndrome - diagnosis | Turner Syndrome - genetics | Angelman Syndrome - blood | Trisomy 13 Syndrome - diagnosis | Chromosome Disorders - genetics | DNA microarrays | Medical screening | Pregnant women | Chromosomes | Analysis | Index Medicus | Abridged Index Medicus
Journal Article
Scientific reports, ISSN 2045-2322, 04/2017, Volume 7, Issue 1, pp. 46434 - 46434
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, pp. e32331 - e32331
Background: Focal Dermal Hypoplasia (FDH) is a genetic disorder characterized by developmental defects in skin, skeleton and ectodermal appendages. FDH is... 
REGULATOR | STEM-CELLS | X-CHROMOSOME | POLARITY GENE PORCUPINE | MID/HINDBRAIN ORGANIZER | MULTIDISCIPLINARY SCIENCES | MOUSE EMBRYOS | MUTATIONS | SPECIFICATION | SECRETION | BETA-CATENIN | Wnt3A Protein - secretion | Humans | Zygote - metabolism | Gene Expression Profiling | Genes, Lethal | Gene Expression Regulation, Developmental | Gene Deletion | Membrane Proteins - metabolism | Disease Models, Animal | Acyltransferases | Cell Line | Gene Targeting | Focal Dermal Hypoplasia - metabolism | Breeding | Introns | Membrane Proteins - genetics | Mice, Inbred C57BL | Gene Silencing | Focal Dermal Hypoplasia - genetics | Gene Knockout Techniques | Mice, Knockout | Phenotype | Animals | Mice | Chimera | Proteins | Embryonic development | Analysis | Drosophila | Stem cells | Skin | Antibacterial agents | Pediatrics | Animal models | Wnt protein | Mesenchyme | Homeostasis | Genomes | Lethality | Focal dermal hypoplasia | Recombinase | Inactivation | Defects | Clonal deletion | Dentition | Deletion | Appendages | Hypoplasia | Deactivation | Baldness | Secretion | Abnormalities | Gynecology | Teeth | Embryos | Obstetrics | Cre recombinase | Flox | Children & youth | Mutants | Medicine | Nutrition research | Signaling | Alopecia | Molecular modelling | Insects | Cellular biology | Neomycin | Mutation | Females | Endoplasmic reticulum | Evolution & development | Index Medicus
Journal Article