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Trisomy 16 Triploid syndrome Edwards syndrome Trisomy 22 Trisomy 8 Down syndrome Trisomy x Genetics of down syndrome Genetic disorder Proteus syndrome Chromosomal deletion syndrome 13q deletion syndrome Birth defect Tricuspid atresia Neurofibromatosis Patau syndrome Klinefelter syndrome Jacobsen syndrome Trinucleotide repeat expansion Nephronophthisis Crouzon syndrome Mcleod syndrome Pentasomy x Digeorge syndrome Noninvasive prenatal testing Tetrasomy x Diastrophic dysplasia Congenital heart defect Steatocystoma multiplex Sanfilippo syndrome Atrial septal defect Congenital syphilis Adrenoleukodystrophy Lig4 syndrome Achondroplasia Gonadal dysgenesis Multicystic dysplastic kidney Focal cortical dysplasia Fragile x syndrome Congenital adrenal hyperplasia Polysplenia Turner syndrome Omenn syndrome Fg syndrome Megalencephaly Glycogen storage disease type iii Incontinentia pigmenti Angelman syndrome Mitochondrial disease Methylmalonic acidemia Lethal allele Meconium aspiration syndrome Sotos syndrome Congenital myasthenic syndrome Alagille syndrome Cleidocranial dysostosis Diffuse infantile fibromatosis Cri du chat syndrome Aneuploidy Polyhydramnios Charge syndrome Marfan syndrome Persistent truncus arteriosus Causes of cancer Sickle cell disease Thalassemia Ectopic pregnancy Diffuse neonatal hemangiomatosis Fetal hydantoin syndrome Sex chromosome anomalies Agenesis of the corpus callosum Acrania Neurofibromatosis type i Treacher collins syndrome Harlequin-type ichthyosis Leigh syndrome Esophageal atresia Congenital rubella syndrome 45,x/46,xy mosaicism Apert syndrome Ectodermal dysplasia 46,xx/46,xy Cornelia de lange syndrome Fetal alcohol spectrum disorder Leukocyte adhesion deficiency Branchio-oto-renal syndrome Hirschsprung's disease Stillbirth Tetralogy of fallot Leber congenital amaurosis Schwannomatosis Kallmann syndrome Dyskeratosis congenita Tetra-amelia syndrome Molar pregnancy Cdkn2a Griscelli syndrome Cephalopelvic disproportion Atypical hemolytic uremic syndrome Pentalogy of cantrell

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