Steven D Klein

4PUBLICATIONS
29CO-AUTHORS
Haematological tumoursGene expression (incl. microarray and other genome-wide approaches)Gene mappingCell and nuclear division
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Publications (4)

|Sep 25, 2024
Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith-Wiedemann Syndrome and Other Predisposition Syndromes.

Jennifer M Kalish, Kerri D Becktell, Gaëlle Bougeard

|Aug 19, 2024
Phenotypic spectrum and tumor risk in Simpson-Golabi-Behmel syndrome: Case series and comprehensive literature review.

Alex F Nisbet, Aravind Viswanathan, Andrew M George

|May 13, 2023
Occurrence of Hepatoblastomas in Patients with Beckwith-Wiedemann Spectrum (BWSp).

Steven D Klein, Madison DeMarchis, Rebecca L Linn

|Nov 18, 2018
Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males.

Sureni V Mullegama, Steven D Klein, Rebecca H Signer

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