Imprinted genes in clinical exome sequencing: Review of 538 cases and exploration of mouse-human conservation in the identification of novel human disease loci-Reference-Cited by-同舟云学术

Imprinted genes in clinical exome sequencing: Review of 538 cases and exploration of mouse-human conservation in the identification of novel human disease loci

Published:2020-06 Issue:6 Volume:63 Page:103903
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Bhoj Elizabeth J.,Rajabi Farrah,Baker Samuel W.,Santani Avni,Tan Wen-Hann

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

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4. MAGI2 mutations cause congenital nephrotic syndrome;Bierzynska;J. Am. Soc. Nephrol.,2017

5. Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome;Bischof;Hum. Mol. Genet.,2007

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