A newborn infant with infantile spinal muscular atrophy associated with trisomy 21 and congenital hypothyroidism [3]

Gulcan H.Uzum I.Dayangac D.Gurses I.2024-08-042024-08-0420051015-8146https://hdl.handle.net/11616/90811[No abstract available]eninfo:eu-repo/semantics/closedAccessDNAcase reportcongenital hypothyroidismdisease associationdisease classificationdisease severityDNA sequenceDown syndromehumanhuman tissuelettermalemotor neuron diseasemuscle hypotonianewbornpolymerase chain reactionspinal muscular atrophythyroid functiontrisomy 21AutoantigensCongenital HypothyroidismDown SyndromeEchocardiography, Doppler, ColorExonsHeart Septal Defects, AtrialHumansHypothyroidismInfant, NewbornMaleRibonucleoproteins, Small NuclearSpinal Muscular Atrophies of ChildhoodA newborn infant with infantile spinal muscular atrophy associated with trisomy 21 and congenital hypothyroidism [3]Letter161113114158447902-s2.0-16444380146N/A