Clinical features of microdeletion 9q22.3 (pat)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01141.x/fullpdf
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1. Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype;American Journal of Medical Genetics Part A;2021-05-07
2. Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study;BMC Neuroscience;2020-07-07
3. A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter;European Journal of Medical Genetics;2020-05
4. Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature;Epilepsy & Behavior Reports;2020
5. Wilms Tumor Associated With the 9q22.3 Microdeletion Syndrome: 2 New Case Reports and a Review of The Literature;Journal of Pediatric Hematology/Oncology;2019-11
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