Investigation of (epi) genotype causes and follow‐up manifestations in the patients with classical and atypical phenotype of Beckwith‐Wiedemann spectrum
B Tüysüz, N Güneş, F Geyik, G Yeşil… - American Journal of …, 2021 - Wiley Online Library
Beckwith‐Wiedemann syndrome (BWS) is a genomic imprinting disorder, characterized by
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
Investigation of (epi) genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum
B Tuysuz, N Gunes, F Geyik, G Yesil… - … GENETICS PART A, 2021 - avesis.istanbul.edu.tr
Beckwith-Wiedemann syndrome (BWS) is a genomic imprinting disorder, characterized by
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
Investigation of (epi) genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum
B Tüysüz, N Güneş, F Geyik, G Yeşil… - … journal of medical …, 2021 - pubmed.ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a genomic imprinting disorder, characterized by
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
Investigation of (epi) genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum.
B Tüysüz, N Güneş, F Geyik, G Yeşil, T Celkan… - 2021 - openaccess.bezmialem.edu.tr
Beckwith-Wiedemann syndrome (BWS) is a genomic imprinting disorder, characterized by
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
Investigation of (epi) genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum.
B Tüysüz, N Güneş, F Geyik, G Yeşil… - American Journal of …, 2021 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) is a genomic imprinting disorder, characterized by
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …