Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation

Παρόμοια τεκμήρια

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  ανά: Barnicoat, Angela
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• The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia
  ανά: Pashaei, Mahdieh, κ.ά.
  Έκδοση: (2020)
• VSX2 mutations in autosomal recessive microphthalmia
  ανά: Reis, Linda M., κ.ά.
  Έκδοση: (2011)
• Novel Compound Heterozygous Mutations in CRTAP Cause Rare Autosomal Recessive Osteogenesis Imperfecta
  ανά: Tang, Yen-An, κ.ά.
  Έκδοση: (2020)