Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma-Reference-Cited by-同舟云学术

Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma

Published:2019-08 Issue:8 Volume:62 Page:103701
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Schieffer Kathleen M.,Varga Elizabeth,Miller Katherine E.,Agarwal Vibhuti,Koboldt Daniel C.,Brennan Patrick,Kelly Benjamin,Dave-Wala Ashita,Pierson Christopher R.,Finlay Jonathan L.,AbdelBaki Mohamed S.,White Peter,Magrini Vincent,Wilson Richard K.,Mardis Elaine R.,Cottrell Catherine E.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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4. Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype;Bayrakli;BMC Genet.,2013

5. Myo18b is essential for sarcomere assembly in fast skeletal muscle;Berger;Hum. Mol. Genet.,2017

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