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Congenital, hereditary, and neonatal diseases and abnormalities

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  • Anemia - Hemolytic
  • Anemia - Hemolytic, congenital
  • Angelman syndrome
  • Barrett esophagus
  • Brain diseases - Metabolic, inborn
  • Charcot-Marie-Tooth disease
  • Chromosome disorders
  • Cleft lip
  • Congenital abnormalities
  • Congenital hypothyroidism
  • Congenital, hereditary, and neonatal diseases and abnormalities panel
  • Cystic fibrosis panel
  • Dwarfism
  • Fetal diseases
  • Fetal growth retardation
  • Genetic diseases - Inborn
  • Genetic diseases - X-linked
  • Gestational trophoblastic disease
  • Heart defects - Congenital
  • Hemoglobinopathies
  • Hereditary sensory and motor neuropathy
  • Infant newborn diseases
  • Li-Fraumeni syndrome
  • Lipid metabolism - Inborn errors
  • Marfan syndrome
  • Melas syndrome
  • Mental disorders diagnosed in childhood
  • Metabolism - Inborn errors
  • Neoplastic syndromes - Hereditary
  • Prader-Willi syndrome
  • Urogenital abnormalities
  • Abnormalities - Multiple
  • Anemia
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