A case with complex small supernumerary marker chromosome consisting 19p and 22q

被引：0

作者：

Altiner, S. ^{[1
]}

Kutlay, N. Yurur ^{[1
]}

机构：

[1] Ankara Univ, Sch Med, Dept Med Genet, Ankara, Turkey

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28卷 / SUPPL 1期

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：

P11.21.C

引用

页码：458 / 458

页数：1

共 2 条

[1] Complex small supernumerary marker chromosomes - an update [J].

Liehr, Thomas ;

Cirkovic, Sanja ;

Lalic, Tanja ;

Guc-Scekic, Marija ;

de Almeida, Cynthia ;

Weimer, Joerg ;

Iourov, Ivan ;

Melaragno, Maria Isabel ;

Guilherme, Roberta S. ;

Stefanou, Eunice-Georgia G. ;

Aktas, Dilek ;

Kreskowski, Katharina ;

Klein, Elisabeth ;

Ziegler, Monika ;

Kosyakova, Nadezda ;

Volleth, Marianne ;

Hamid, Ahmed B. .

MOLECULAR CYTOGENETICS, 2013, 6

[2] Pure Duplication of 19p13.3 in Three Members of a Family with Intellectual Disability and Literature Review. Definition of a New Microduplication Syndrome [J].

Orellana, Carmen ;

Rosello, Monica ;

Monfort, Sandra ;

Mayo, Sonia ;

Oltra, Silvestre ;

Martinez, Francisco .

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (07) :1614-1620

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