A newborn infant with infantile spinal muscular atrophy associated with trisomy 21 and congenital hypothyroidism [3]
Küçük Resim Yok
Tarih
2005
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
[No abstract available]
Açıklama
Anahtar Kelimeler
DNA, case report, congenital hypothyroidism, disease association, disease classification, disease severity, DNA sequence, Down syndrome, human, human tissue, letter, male, motor neuron disease, muscle hypotonia, newborn, polymerase chain reaction, spinal muscular atrophy, thyroid function, trisomy 21, Autoantigens, Congenital Hypothyroidism, Down Syndrome, Echocardiography, Doppler, Color, Exons, Heart Septal Defects, Atrial, Humans, Hypothyroidism, Infant, Newborn, Male, Ribonucleoproteins, Small Nuclear, Spinal Muscular Atrophies of Childhood
Kaynak
Genetic Counseling
WoS Q Değeri
Scopus Q Değeri
N/A
Cilt
16
Sayı
1
