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Academic Journal

High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.

Subjects: GENETIC mutation; BLOOD coagulation factor XIII; GENOTYPES

  • Source: Haemophilia. Nov2017, Vol. 23 Issue 6, pe488-e496. 9p.

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Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo.

  • Authors : Bravo-Pérez C; Servicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, University of Murcia, IMIB-Arrixaca, CIBERER, Murcia, Spain.; de la Morena-Barrio ME

Subjects: Family* ; Fetal Death* ; Genotype*

  • Source: British journal of haematology [Br J Haematol] 2020 Oct; Vol. 191 (1), pp. e32-e35. Date of Electronic Publication: 2020 Jul 19.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium:

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  • 1-2 of  2 results for ""la Morena‐Barrio, M. E.""