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Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome

机译：复杂的遗传模式类似于常染色体隐性遗传，涉及血小板减少症-无Rad综合征的微缺失

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Klopocki Eva; Schulze Harald; Strauß Gabriele; Ott Claus-Eric; Hall Judith; Trotier Fabienne; Fleischhauer Silke; Greenhalgh Lynn; Newbury-Ecob Ruth A.; Neumann Luitgard M.; Habenicht Rolf; König Rainer; Seemanova Eva; Megarbane André; Ropers Hans-Hilger; Ullmann Reinhard; Horn Denise; Mundlos Stefan;
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1. Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case [J] . Elisa Tassano, Stefania Gimelli, Maria Teresa Divizia, Molecular cytogenetics . 2015 ,第1期

机译：由于1Q21.1微缺失的化合物遗传和低频非涂布RBM8A SNP，血小板减少症综合征（焦油）综合征
2. Small-platelet thrombocytopenia in a family with autosomal recessive inheritance pattern [J] . Levin Carina, Zalman Lucia, Tamary Hannah, Pediatric blood & cancer . 2013 ,第10期

机译：具有常染色体隐性遗传方式的家庭中的小血小板血小板减少症
3. Gómez-lópez-hernández syndrome in a child born to consanguineous parents: New evidence for an autosomal-recessive pattern of inheritance? [J] . DeMattosV.F., GraziadioC., PortoAlegreRSBrazil, Pediatric neurology . 2014 ,第6期

机译：血缘父母所生孩子中的Gómez-lópez-hernández综合征：常染色体隐性遗传的新证据吗？
4. Recessive Trait Cross over Approach of GAs Population Inheritance for Evolutionary Optimization [C] . Amr Madkour, Alamgir Hossain, Keshav Dahal Online World Conference on Soft Computing in Industrial Applications . 2007

机译：隐性特性交叉过于煤气种群遗传方法的进化优化
5. Fashioning spatial identity: A work environment and showroom for a fashion marketer with Thrombocytopenia Absent Radius syndrome: Dusseldorf, Germany. [D] . Brunel, Celeste. 2007

机译：塑造时尚的空间身份：患有血小板减少症而无半径综合征的时尚商人的工作环境和陈列室：德国杜塞尔多夫。
6. Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome [O] . Eva Klopocki, Harald Schulze, Gabriele Strauß, 2007

机译：复杂的遗传模式类似于常染色体隐性遗传涉及血小板减少症-无Rad综合征的微缺失
7. Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case [O] . 2015

机译：由于1q21.1微缺失和低频非编码RBM8A SNP的复合遗传而导致的血小板减少症无radius骨（TAR）综合征：一个新的家族病例

Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome

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