Cryptic insertion of KMT2A, a rare t(9;11) variant. | Blood;137(13): 1843, 2021 04 01. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Search Portal

Information and Knowledge for Health

Subject descriptor lookup Advanced Search

Cryptic insertion of KMT2A, a rare t(9;11) variant.

Assaf, Nada; Terré, Christine.

Affiliation

Assaf N; Centre Hospitalier Mignot.
Terré C; Centre Hospitalier Mignot.

Blood ; 137(13): 1843, 2021 04 01.

Article in En | MEDLINE | ID: mdl-33792681

Subject(s)

Histone-Lysine N-Methyltransferase/genetics; Myeloid-Lymphoid Leukemia Protein/genetics; Pancytopenia/genetics; Aged; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 9; Humans; INDEL Mutation; Male; Translocation, Genetic

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancytopenia / Histone-Lysine N-Methyltransferase / Myeloid-Lymphoid Leukemia Protein Limits: Aged / Humans / Male Language: En Journal: Blood Year: 2021 Type: Article

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancytopenia / Histone-Lysine N-Methyltransferase / Myeloid-Lymphoid Leukemia Protein Limits: Aged / Humans / Male Language: En Journal: Blood Year: 2021 Type: Article