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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
Journal Article
EBioMedicine, ISSN 2352-3964, 08/2015, Volume 2, Issue 8, pp. 968 - 984
Journal Article
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 07/2008, Volume 93, Issue 7, pp. 2800 - 2805
Journal Article
Clinical Genetics, ISSN 0009-9163, 02/2018, Volume 93, Issue 2, pp. 216 - 222
Background: Individuals with fragile X syndrome (FXS) have both behavioral and medical comorbidities and the latter include obesity in approximately 30% and... 
metformin | targeted treatments | obesity | fragile X syndrome | Prader‐Willi‐phenotype | Prader-Willi-phenotype | CHILDREN | THERAPY | ADOLESCENTS | GENETICS & HEREDITY | DOUBLE-BLIND | PEOPLE | PLACEBO-CONTROLLED TRIAL | PRADER-WILLI PHENOTYPE | Mental Disorders - pathology | Obesity - drug therapy | Diabetes Mellitus, Type 2 - genetics | Glycated Hemoglobin A - metabolism | Humans | Middle Aged | Child, Preschool | Fragile X Syndrome - pathology | Male | Glucose Intolerance - pathology | Obesity - blood | Obesity - genetics | Fragile X Syndrome - drug therapy | Glucose Intolerance - blood | Young Adult | Glucose Intolerance - drug therapy | Prader-Willi Syndrome - genetics | Adult | Female | Metformin - administration & dosage | Child | Prader-Willi Syndrome - drug therapy | Fragile X Syndrome - genetics | Glucose Intolerance - genetics | Prader-Willi Syndrome - blood | Mental Disorders - blood | Fragile X Syndrome - blood | Treatment Outcome | Obesity - pathology | Diabetes Mellitus, Type 2 - blood | Animals | Prader-Willi Syndrome - pathology | Mental Disorders - drug therapy | Diabetes Mellitus, Type 2 - pathology | Diabetes Mellitus, Type 2 - drug therapy | Type 2 diabetes | Prader-Willi syndrome | Comorbidity | Analysis | Glycosylated hemoglobin | Fragile X syndrome | Metformin | Glucose | Children | Health aspects | Dextrose | Diabetes therapy | Obesity | Hyperactivity | Diabetes mellitus | Mental retardation | Glucose tolerance | Language | Behavior | Diabetes | Diabetes mellitus (non-insulin dependent) | Hyperphagia
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 03/2012, Volume 97, Issue 3, pp. E452 - E459
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 12/2002, Volume 87, Issue 12, pp. 5461 - 5464
Prader-Willi syndrome (PWS) is a genetic disorder occurring in 1 of 10,000–16,000 live births and is characterized by excessive appetite with progressive... 
HUMANS | ENDOCRINOLOGY & METABOLISM | Hyperphagia - etiology | Prader-Willi Syndrome - blood | Humans | Peptide Hormones - blood | Male | Reference Values | Prader-Willi Syndrome - complications | Eating - physiology | Osmolar Concentration | Fasting - blood | Ghrelin | Prader-Willi Syndrome - physiopathology | Adult | Female | Obesity - etiology | Hunger - physiology
Journal Article