Publications
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is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. . .
is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. .
is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia. J Transl Med. 2015 ;13:179.
. Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia. J Transl Med. 2015 ;13:179.
. . . is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. . .
is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
. . .
is mutated in a distinct type of Usher syndrome. J Med Genet. 2017 ;54(3):190-195.
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