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2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
Eun-Kyung Cho, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2017;22(2):129-132.   Published online June 28, 2017
DOI: https://doi.org/10.6065/apem.2017.22.2.129

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2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
Annals of Pediatric Endocrinology & Metabolism. 2017;22(2):129   Crossref logo
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Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size
American Journal of Medical Genetics Part A. 2016;170(9):2282-2291   Crossref logo
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1p36 deletion syndrome confirmed by fluorescencein situhybridization and array-comparative genomic hybridization analysis
Korean Journal of Pediatrics. 2016;59(Suppl 1):S14   Crossref logo
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Angelman syndrome: Validation of molecular cytogenetic analysis of chromosome 15q11-q13 for deletion detection
American Journal of Medical Genetics. 1995;56(1):101-105   Crossref logo
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Medullary thyroid carcinoma and 2q37 deletion in a patient with nevoid basal cell carcinoma syndrome: Clinical description and genetic analysis
Head & Neck. 2012;35(5):E147-E152   Crossref logo
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High-resolution cytogenetic studies in patients with Prader-Willi syndrome
Clinical Genetics. 2008;30(4):241-248   Crossref logo
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22q and two: 22q11.2 deletion syndrome and coexisting conditions
American Journal of Medical Genetics Part A. 2018;176(10):2203-2214   Crossref logo
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Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome
American Journal of Medical Genetics Part A. 2018;176(10):2099-2103   Crossref logo
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Deletion or triplication of the α3(VI) collagen gene in three patients with 2q37 chromosome aberrations and symptoms of collagen-related disorders
Clinical Genetics. 2008;49(6):279-285   Crossref logo
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Clinical phenotype associated with terminal 2q37 deletion
Clinical Genetics. 2008;48(3):134-139   Crossref logo
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