Connection

Zain Bassam Mohammad DARDAS to Male

This is a "connection" page, showing publications Zain Bassam Mohammad DARDAS has written about Male.
Connection Strength

0.052
  1. The impact of exome sequencing on the diagnostic yield of muscular dystrophies in consanguineous families. Eur J Med Genet. 2020 Apr; 63(4):103845.
    View in: PubMed
    Score: 0.021
  2. Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies. Genes (Basel). 2021 04 19; 12(4).
    View in: PubMed
    Score: 0.006
  3. Enteric anendocrinosis attributable to a novel Neurogenin-3 variant. Eur J Med Genet. 2020 Sep; 63(9):103981.
    View in: PubMed
    Score: 0.005
  4. Clinical heterogeneity in retinitis pigmentosa caused by variants in RP1 and RLBP1 in five extended consanguineous pedigrees. Mol Vis. 2020; 26:445-458.
    View in: PubMed
    Score: 0.005
  5. Extending the spectrum of CLRN1- and ABCA4-associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. Mol Genet Genomic Med. 2020 03; 8(3):e1123.
    View in: PubMed
    Score: 0.005
  6. The frequency of NOTCH1 variants in T-acute lymphoblastic leukemia/lymphoma and chronic lymphocytic leukemia/small lymphocytic lymphoma among Jordanian patients. Ann Diagn Pathol. 2019 Apr; 39:53-58.
    View in: PubMed
    Score: 0.005
  7. Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies. Can J Ophthalmol. 2019 02; 54(1):51-59.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.