Somatic mosaicism inMYH9disorders: the need to carefully evaluate apparently healthy parents

Apparent genotype–phenotype mismatch in a patient with MYH9-related disease: When the exception proves the rule

(2013) Daniela De Rocco et al.   THROMBOSIS AND HAEMOSTASIS

Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure: case report and review of the literature

(2012) Mami Ishida et al.   CLINICAL NEPHROLOGY

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias

(2011) Carlo L. Balduini et al.   BRITISH JOURNAL OF HAEMATOLOGY

Advances in the understanding of MYH9 disorders

(2010) Shinji Kunishima et al.   CURRENT OPINION IN HEMATOLOGY

Germinal mosaicism inMYH9disorders: a family with two affected siblings of normal parents

(2009) Shinji Kunishima et al.   BRITISH JOURNAL OF HAEMATOLOGY

Identification of three in-frame deletion mutations inMYH9disorders suggesting an important hot spot for small rearrangements inMYH9exon 24

(2009) Koji Miyazaki et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Identification of the first duplication in MYH9-related disease: A hot spot for unequal crossing-over within exon 24 of the MYH9 gene

(2009) Daniela De Rocco et al.   European Journal of Medical Genetics