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chromosomal microarray analysis–single nucleotide polymorphism array
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Select article: Prader-Willi Syndrome With a Long-Contiguous Stretch of Homozygosity Not Covering the Critical Region
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Research article
First published March, 2015
Prader-Willi Syndrome With a Long-Contiguous Stretch of Homozygosity Not Covering the Critical Region
Xie Yingjun,
Zhou Yi,
Wu Jianzhu
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Journal of Child Neurology
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Select article: De Novo 1.77-Mb Microdeletion of 10q22.2q22.3 in a Girl with Developmental Delay,Speech Delay,Congenital Cleft Palate,and Bilateral Hearing Impairment
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Case report
First published May, 2017
De Novo 1.77-Mb Microdeletion of 10q22.2q22.3 in a Girl with Developmental Delay,Speech Delay,Congenital Cleft Palate,and Bilateral Hearing Impairment
Ting-Ying Lei,
Hong-Tao Wang,
Fan Li
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The Cleft Palate Craniofacial Journal
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Select article: Is Chromosome 15q13.3 Duplication Involving CHRNA7 Associated With Oral Clefts?
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Research article
First published December, 2015
Is Chromosome 15q13.3 Duplication Involving CHRNA7 Associated With Oral Clefts?
Yingjun Xie
Child Neurology Open
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