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8. Genetic heterogeneity in Pakistani microcephaly families revisited

11. Body composition and plasma lipid and stress hormone levels during 3 weeks of feed restriction and refeeding in low birth weight female pigs

23. First HPSE2 missense mutation in urofacial syndrome

33. Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21‐q23

41. A new form of spinal muscular atrophy

42. Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia

43. Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

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