Ritscher-Schinzel syndrome: broadening the phenotype in prenatal and adulthood

被引：0

作者：

Nery, Sabrina ^{[1
,2
]}

Maia, Nuno ^{[3
,4
]}

Fortuna, Ana Maria ^{[3
,4
,5
]}

Damasio, Joana ^{[4
,5
,6
,7
,8
]}

Coale, Elizabeth ^{[9
]}

Willisi, Mary ^{[10
]}

Jorge, Paula ^{[3
,4
,5
]}

Hojte, Anne F. ^{[1
]}

Fenger, Christina Duhring ^{[1
,11
]}

Moeller, Rikke Steensbjerre ^{[1
,12
]}

Bayat, Allan ^{[1
,12
]}

机构：

[1] Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Med, Dianalund, Denmark

[2] Magna Graecia Univ Catanzaro, Dept Med & Surg Sci, Catanzaro, Italy

[3] Ctr Hosp Univ Santo Antonio CHUdSA, Ctr Genet Med Jacinto Magalhaes CGM, Porto, Portugal

[4] Univ Porto, ICBAS Sch Med & Biomed Sci, UMIB Unit Multidisciplinary Res Biomed, Porto, Portugal

[5] ITR Lab Integrat & Translat Res Populat Hlth, Porto, Portugal

[6] Ctr Hosp Univ Santo Antonio CHUdSA, Serv Neurol, Porto, Portugal

[7] Univ Porto, Inst Biol Mol & Celular, CGPP, i3S Inst Invest & Inovacao Saude, Porto, Portugal

[8] Univ Porto, UnIGENE, Inst Invest & Inovacao Saude i3S, Porto, Portugal

[9] Univ Washington, Dept Maternal Fetal Med, Med Ctr, Seattle, WA USA

[10] Naval Med Ctr San Diego, Dept Pediat, San Diego, CA USA

[11] Amplexa Genet AS, Odense, Denmark

[12] Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32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：

P12.037.B

引用

页码：538 / 538

页数：1

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