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Otology and Neurotology, ISSN 1531-7129, 12/2008, Volume 29, Issue 8, pp. 1209 - 1210
Trisomy 13 syndrome Occurs in approximately 1 in 5,000 live births with Multiple congenital anomalies. The most common otolaryngologic findings are apneic... 
TEMPORAL BONE | OTORHINOLARYNGOLOGY | CLINICAL NEUROLOGY | Ear Canal - pathology | Trisomy - genetics | Connective Tissue - pathology | Humans | Stillbirth | Chromosomes, Human, Pair 13 | Female | Trisomy - pathology | Abnormalities, Multiple - genetics | Infant, Newborn | Index Medicus
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 06/2018, Volume 20, Issue 6, p. 485
A girl aged 5 months was admitted due to developmental delay. Physical examination showed delayed physical development, unusual facies (microcephalus,... 
Chromosome Deletion | Chromosomes, Human, Pair 13 - genetics | Phenotype | Trisomy - genetics | Comparative Genomic Hybridization | Humans | Female | Infant | Ring Chromosomes
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
Journal Article
Laryngoscope, ISSN 0023-852X, 03/2008, Volume 118, Issue 3, pp. 506 - 507
The temporal bones of a 23-week-old female who had multiple congenital anomalies and bilateral hearing loss with trisomy 13 syndrome were evaluated under light... 
Human temporal bone | Trisomy 13 syndrome | Histopathology | human temporal bone | MEDICINE, RESEARCH & EXPERIMENTAL | histopathology | OTORHINOLARYNGOLOGY | Chromosomes, Human, Pair 13 | Temporal Bone - pathology | Female | Infant | Trisomy | Humans | Index Medicus
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2013, Volume 161, Issue 10, pp. 2512 - 2518
Journal Article
Journal of Medical Screening, ISSN 0969-1413, 9/2014, Volume 21, Issue 3, pp. 113 - 119
Objectives Pregnancies with Edwards or Patau syndrome are often detected through screening for Down’s syndrome. We aimed to evaluate the impact of screening... 
Trisomy 18 | Prenatal screening | Trisomy 13 | Antenatal detection | Patau syndrome | Edwards syndrome | RISK | MATERNAL AGE | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | BORN | DOWN-SYNDROME | INFANTS | TRISOMIES 13 | Pregnancy | Care and treatment | Analysis | Research | Down syndrome | Diagnosis | Medical screening
Journal Article
Case Reports in Perinatal Medicine, ISSN 2192-8932, 12/2012, Volume 1, Issue 1, pp. 95 - 98
Pseudotrisomy 13 syndrome is determined by the combination of three findings: holoprosencephaly, postaxial polydactyly, and a normal karyotype. We report two... 
trisomy | syndrome | Holoprosencephaly | polydactyly
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2014, Volume 211, Issue 5, pp. 527.e1 - 527.e17
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2014, Volume 370, Issue 9, pp. 799 - 808
Journal Article