Seco, Celia Zazo
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2

Trends in genetic diagnostics of hereditary hearing loss: P..:

Pennings, Ronald ; Seco, Celia Zazo ; Wesdorp, Mieke...
The Journal of Laryngology & Otology.  130 (2016)  S3 - p. S27-S27 , 2016
 
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De Novo Missense Variants in FBXW11 Cause Diverse Developme..:

Holt, Richard J. ; Young, Rodrigo M. ; Crespo, Berta...
The American Journal of Human Genetics.  105 (2019)  3 - p. 640-657 , 2019
 
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6

The diagnostic yield of whole-exome sequencing targeting a ..:

Zazo Seco, Celia ; Wesdorp, Mieke ; Feenstra, Ilse...
European Journal of Human Genetics.  25 (2016)  3 - p. 308-314 , 2016
 
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7

The diagnostic yield of whole-exome sequencing targeting a ..:

Seco, Celia Zazo ; Wesdorp, Mieke ; Feenstra, Ilse...
Seco , C Z , Wesdorp , M , Feenstra , I , Pfundt , R , Hehir-Kwa , J Y , Lelieveld , S H , Castelein , S , Gilissen , C , de Wijs , I J , Admiraal , R J C , Pennings , R J E , Kunst , H P M , van de Kamp , J M , Tamminga , S , Houweling , A C , Plomp , A S , Maas , S M , Gans , P A M D K , Kant , S G , de Geus , C M , Frints , S G M , Vanhoutte , E K , van Dooren , M F , van den Boogaard , M-J H , Scheffer , H , Nelen , M , Kremer , H , Hoefsloot , L , Schraders , M & Yntema , H G 2017 , ' The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands ' , European Journal of Human Genetics , vol. 25 , no. 3 , pp. 308-314 . https://doi.org/10.1038/ejhg.2016.182.  , 2017
 
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A homozygous FITM2 mutation causes a deafness-dystonia synd..:

Seco, Celia Zazo ; Castells-Nobau, Anna ; Joo, Seol-hee...
Seco , C Z , Castells-Nobau , A , Joo , S , Schraders , M , Foo , J N , van der Voet , M , Velan , S S , Nijhof , B , Oostrik , J , de Vrieze , E , Katana , R , Mansoor , A , Huynen , M , Szklarczyk , R , Oti , M , Tranebjaerg , L , van Wijk , E , Scheffer-de Gooyert , J M , Siddique , S , Baets , J , de Jonghe , P , Kazmi , S A R , Sadananthan , S A , van de Warrenburg , B P , Khor , C C , Goepfert , M C , Qamar , R , Schenck , A , Kremer , H & Siddiqi , S 2017 , ' A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy ' , Disease Models & Mechanisms , vol. 10 , no. 2 , pp. 105-118 . https://doi.org/10.1242/dmm.026476.  , 2017
 
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