Concepedia

Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia

Michael Kirwan, Amanda J. Walne, Vincent Plagnol, Mark Velangi, Aloysius Ho, Upal Hossain, Tom Vulliamy, Inderjeet Dokal

The American Journal of Human Genetics · 2012 · 118 citations · 14 references

DOIFull text

Open access

Concepts

References

14

Parametric and nonparametric linkage analysis: a unified multipoint approach.

Leonid Kruglyak, Mark J. Daly, Mary Pat Reeve-Daly et al. · PubMed · 1996 · 2.9K citations · Full text

, , +7

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

Woo‐Joo Song, Melanie G. Sullivan, Robert D. Legare et al. · Nature Genetics · 1999 · 1.1K citations

, , +8

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

Christopher N Hahn, Chan‐Eng Chong, Catherine Carmichael et al. · Nature Genetics · 2011 · 601 citations · Full text

, , +16

Identification of eight members of the Argonaute family in the human genome☆

Takashi Sasaki, Aiko Shiohama, Nobuyoshi Shimizu · Genomics · 2003 · 410 citations

, , +8

Mutation of<i>CEBPA</i>in Familial Acute Myeloid Leukemia

Matthew L. Smith, Jamie Cavenagh, Tim Lister et al. · New England Journal of Medicine · 2004 · 327 citations

, , +11