Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome Journal Article


Authors: Schwartz, J. R.; Wang, S.; Ma, J.; Lamprecht, T.; Walsh, M.; Song, G.; Raimondi, S. C.; Wu, G.; Walsh, M. F.; McGee, R. B.; Kesserwan, C.; Nichols, K. E.; Cauff, B. E.; Ribeiro, R. C.; Wlodarski, M.; Klco, J. M.
Article Title: Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome
Keywords: child; preschool child; unclassified drug; somatic mutation; neutropenia; case report; letter; thrombocytopenia; protein; disease severity; myelodysplastic syndrome; heterozygosity loss; sibling; disease predisposition; chromosome analysis; karyotype; thrombocyte transfusion; germline mutation; hypospadias; megalocytosis; monosomy 7; sanger sequencing; human; male; priority journal; whole genome sequencing; samd9 protein
Journal Title: Leukemia
Volume: 31
Issue: 8
ISSN: 0887-6924
Publisher: Nature Publishing Group  
Date Published: 2017-08-01
Start Page: 1827
End Page: 1830
Language: English
DOI: 10.1038/leu.2017.142
PROVIDER: scopus
PMCID: PMC5540771
PUBMED: 28487541
DOI/URL:
Notes: Letter -- Export Date: 5 September 2017 -- Source: Scopus
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  1. Michael Francis Walsh
    145 Walsh