Benefits of whole exome sequencing to advance the genetic diagnosis in patients with differences (disorders) of sex development

被引：0
|
作者：
Syryn, Hannes [1 ]
Verdin, Hannah [1 ]
De Velde, Julie Van [1 ]
Becker, Marianne [2 ]
Brachet, Cecile [3 ]
den Brinker, Marieke [4 ]
Depoorter, Sylvia [5 ]
Fudvoye, Julie [6 ]
Klink, Daniel [7 ]
Lysy, Philippe [8 ]
Massa, Guy [9 ]
Reynaert, Nele [10 ]
Rochtus, Anne [10 ]
Staels, Willem [11 ]
Van Loocke, Marlies [10 ]
Cools, Martine [12 ]
De Baere, Elfride [1 ]
机构：
[1] Ghent Univ Hosp, Dept Biomol Med, Ctr Med Genet, Ghent, Belgium
[2] Ctr Hosp Luxembourg, Pediat Endocrinol & Diabetol DECCP, Luxembourg, Luxembourg
[3] Hop Univ Enfants Reine Fabiola, Paediat Endocrinol Unit, Brussels, Belgium
[4] Antwerp Univ Hosp, Dept Paediat Endocrinol, Antwerp, Belgium
[5] Gen Hosp Sint Jan Bruges Ostend, Dept Child Endocrinol, Brugge, Belgium
[6] CHU Liege, Dept Pediat, Liege, Belgium
[7] ZNA Queen Paola Childrens Hosp, Div Pediat Endocrinol & Diabet, Antwerp, Belgium
[8] Clin Univ St Luc, Pediat Endocrinol, Brussels, Belgium
[9] Jessa Hosp, Dept Pediat Endocrinol & Diabetol, Hasselt, Belgium
[10] Univ Hosp Leuven, Dept Paediat Endocrinol, Leuven, Belgium
[11] Univ Hosp Brussels, Div Pediat Endocrinol, Jette, Belgium
[12] Ghent Univ Hosp, Dept Internal Med & Pediat, Ghent, Belgium
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P04.027.B
引用
收藏
页码：382 / 383
页数：2
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