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Filiz Hazan

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 7, 2019

Childhood onset limb-girdle muscular dystrophies in the Aegean part of TurkeyUluç Yiş, Gülden Diniz, Filiz Hazan, et al.

European Journal of Human Genetics : EJHG|November 28, 2013

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutationsGabriela E Jones, Pia Ostergaard, Anthony T Moore, et al.

American Journal of Human Genetics|December 1, 2014

Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.

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Search research articles

Showing results (51-60 of 53) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 53 results.

Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 7, 2019

Childhood onset limb-girdle muscular dystrophies in the Aegean part of TurkeyUluç Yiş, Gülden Diniz, Filiz Hazan, et al.

European Journal of Human Genetics : EJHG|November 28, 2013

American Journal of Human Genetics|December 1, 2014

Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.

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