Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable features

被引：0
|
作者：
Awwad, Johnny [1 ]
Yammine, Tony [2 ]
Hamdar, Layal [1 ]
Souaid, Mirna [2 ]
Farra, Chantal [2 ,3 ,4 ]
机构：
[1] Amer Univ Beirut, ObGyn Dept, Fertil Unit, Med Ctr, Beirut, Lebanon
[2] St Joseph Univ, Genet Dept, Med Genet Unit, Beirut, Lebanon
[3] Hotel Dieu de France Univ Hosp, Med Genet Dept, Beirut, Lebanon
[4] St Joseph Univ Beirut, Genet Dept, Med Genet Unit, BP17 5208 Mar Mikhael, Beirut 11042020, Lebanon
来源：
CLINICAL DYSMORPHOLOGY | 2023年 / 32卷 / 02期
关键词：
D O I：
10.1097/MCD.0000000000000447
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：80 / 83
页数：4
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