Search

Author/Creator Mittal Balraj Academic Editor.

42. The Missing LNK: Evolution from Cytosis to Chronic Myelomonocytic Leukemia in a Patient with Multiple Sclerosis and Germline SH2B3 Mutation. (1st March 2022)

Authors:
Gundabolu, Krishna; Dave, Bhavana J.; Alvares, Carmelita J.; Cannatella, Jeffrey J.; Bhatt, Vijaya R.; Maness, Lori J.; Al-Kadhimi, Zaid S.; Zabad, Rana K.; Cushman-Vokoun, Allison M.
Other Names:
Mittal Balraj Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2022(2022)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

44. Whole Exome Sequencing Leading to the Diagnosis of Dysferlinopathy with a Novel Missense Mutation (c.959G>C). (19th April 2016)

Authors:
Swaika, Abhisek; Boczek, Nicole J.; Sood, Neha; Guthrie, Kimberly; Klee, Eric W.; Agrawal, Ankit; Dimberg, Elliot L.; Ailawadhi, Sikander
Other Names:
Mittal Balraj Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2016(2016)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗