author-photo

Manar As'sad

United States Atomic Energy Commission

4

Papers

2

Citations

Citation Trend

Filter By

Papers (4) Sort By

Journal Conference Others

A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome

2020
Show All
- Source
- Cite
- Save
Citations (0)
A De Novo Childhood Case of T-cell Lymphoblastic Leukemia with High Hyperdiploid Karyotype Carrying an Unreported Balanced Translocation t(X;5)(q26;q31.3~32) in A Male Patient

2018
Show All
- Source
- Cite
- Save
Citations (0)
Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report

2017 Journal of Medical Case Reports
Show All
- Source
- Cite
- Save
Citations (1)
A new complex karyotype in a unique de novo myelodysplastic syndrome case involving ten chromosomes and monoallelic loss of TP53

2016 Gene Reports
Show All
- Source
- Cite
- Save
Citations (1)