home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 305      Small font sizeDefault font sizeIncrease font size Print this page Email this page
This article has been cited by
1Biallelic PMS2 Mutation and Heterozygous DICER1 Mutation Presenting as Constitutional Mismatch Repair Deficiency With Corpus Callosum Agenesis: Case Report and Review of Literature
Cletus Cheyuo,Walid Radwan,Janice Ahn,Kymberly Gyure,Rabia Qaiser,Patrick Tomboc
Journal of Pediatric Hematology/Oncology.2017;39(7)e381
[DOI]
2Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)
Katharina Wimmer,Christian P Kratz,Hans F A Vasen,Olivier Caron,Chrystelle Colas,Natacha Entz-Werle,Anne-Marie Gerdes,Yael Goldberg,Denisa Ilencikova,Martine Muleris,Alex Duval,Noémie Lavoine,Clara Ruiz-Ponte,Irene Slavc,Brigit Burkhardt,Laurence Brugieres
Journal of Medical Genetics.2014;51(6)355
[DOI]
3Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1
K. Rerat,F. Parker,G. Nasser,D. Vidaud,F. Riant,E. Tournier-Lasserve,C. Denier
Journal of the Neurological Sciences.2015;350(1-2)98
[DOI]
4Hereditary Multiple Cerebral Cavernous Malformations Associated with Wilson Disease and Multiple Lipomatosis
Olga B. Belousova,Dmitry N. Okishev,Tatyana M. Ignatova,Maria S. Balashova,Eugenia S. Boulygina
World Neurosurgery.2017;105(1-2)1034.e1
[DOI]
5Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1
K. Wimmer,T. Rosenbaum,L. Messiaen
Clinical Genetics.2017;91(4)507
[DOI]
Submit Articles
  Site Statistics 
  Addresses 
  Search 
  My Preferences 
  Online Submission 

Submit Articles

Alerts