Associated Papers
Fibrinogen Deficiency with Thrombotic Manifestations.
Tamayo-Velasco Á et al.
European Journal of Case Reports in Internal Medicine, 2022
UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly.
Schnur RE et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
34040189 (PubMed )
Supplement: NIHMS1717832-supplement-Supplementary___Appendix__online_only_material__etc__.pdf
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