9 research outputs found
Diagnostic exome sequencing for patients with a family history of consanguinity: over 38% of positive results are not autosomal recessive pattern
No full textHigh Prevalence of Congenital Hypothyroidism in the Greek Cypriot Population: Results of the Neonatal Screening Program 1990- 2000
No full textHematological and demographic profile of Pakistani children with isolated ventricular septal defects (VSDs)
No full textCord Blood Thyroxine and Thyroid Stimulating Hormone Screening for Congenital Hypothyroidism: How Useful Are They?
No full textPatterns, prevalence, risk factors, and survival of newborns with congenital heart defects in a Saudi population: a three-year, cohort case-control study
No full textAvaliação do programa de triagem para o hipotireoidismo congênito no estado de Sergipe
No full text
