[HTML][HTML] Molecular basis of Beckwith–Wiedemann syndrome spectrum with associated tumors and consequences for clinical practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - mdpi.com
Simple Summary Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn
overgrowth disorder caused by molecular alterations in chromosome 11p15. 5. These …

Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - publications.aston.ac.uk
Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting condition
with a heterogenous clinical presentation of overgrowth and an increased childhood cancer …

Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - research.aston.ac.uk
Abstract Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting
condition with a heterogenous clinical presentation of overgrowth and an increased …

Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - search.ebscohost.com
Abstract Simple Summary: Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an
inborn overgrowth disorder caused by molecular alterations in chromosome 11p15. 5 …

Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.

T Eggermann, ER Maher, CP Kratz, D Prawitt - 2022 - repository.cam.ac.uk
Abstract Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting
condition with a heterogenous clinical presentation of overgrowth and an increased …

Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - europepmc.org
Abstract Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting
condition with a heterogenous clinical presentation of overgrowth and an increased …

Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - search.proquest.com
Abstract Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting
condition with a heterogenous clinical presentation of overgrowth and an increased …

Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - pubmed.ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting condition
with a heterogenous clinical presentation of overgrowth and an increased childhood cancer …

[HTML][HTML] Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - ncbi.nlm.nih.gov
Abstract Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is a congenital imprinting
condition with a heterogenous clinical presentation of overgrowth and an increased …