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Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH

机译：CDH患者染色体1Q41Q42.12区的表征和候选基因DISP1

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Sibel Kantarci; Kate G. Ackerman; Meaghan K. Russell; Mauro Longoni; Carrie Sougnez; Kristin M. Noonan; Eli Hatchwell; Xiaoyun Zhang; Rafael Pieretti Vanmarcke; Kwame Anyane-Yeboa; Paul Dickman; Jay Wilson; Patricia K. Donahoe; Barbara R. Pober;
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1. Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH. [J] . Kantarci S, Ackerman KG, Russell MK, American journal of medical genetics, Part A . 2010,第10期

机译：CDH患者的染色体1q41q42.12区和候选基因DISP1的特征。
2. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2. [J] . Slavotinek AM, Moshrefi A, Davis R, European journal of human genetics: EJHG . 2006,第9期

机译：先天性diaphragm肌疝患者的阵列比较基因组杂交：四个CDH关键区域的定位和15q26.1-15q26.2候选基因的测序。
3. Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2. [J] . Hadano S, Yanagisawa Y, Skaug J, Genomics . 2001,第2期

机译：在染色体2q33-q34的青少年肌萎缩性侧索硬化症（ALS2）关键区域中，对三个新基因ALS2CR1，ALS2CR2和ALS2CR3进行克隆和鉴定：ALS2的候选基因。
4. Initial study of candidate genes on chromosome two for relative hand skill [C] . C. Phillips, A. Barbara, M.V. Lareu, International Society for Forensic Genetics . 2006

机译：染色体两种候选基因的初步研究
5. A genetic association study of reading disabilities and attention deficit hyperactivity disorder with a candidate region on chromosome 6p and a gene on chromosome 1p [D] . Couto, Jillian Michelle 2008

机译：阅读障碍和注意力缺陷多动障碍的遗传关联研究，其候选区域位于6p号染色体上，而一个基因位于1p号染色体上
6. Characterization of the Chromosome 1q41q42.12 region and the Candidate Gene DISP1 in Patients with CDH [O] . Sibel Kantarci, Kate G Ackerman, Meaghan N Russell, -1

机译：CDH患者染色体1Q41Q42.12区的表征和候选基因DISP1
7. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1–15q26.2 [O] . Anne M Slavotinek, Ali Moshrefi, Randy Davis, 2006

机译：先天性膈疝患者的阵列比较基因组杂交：15〜26.1-15〜15〜15〜5〜15〜15季度候选基因测定的映射。

Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH

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