Phenotype–genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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1. Clinical outcomes of fetuses with chromosome 16 short arm copy number variants;Molecular Genetics & Genomic Medicine;2023-04-04
2. Noniron deficiency microcytic anemia, dysmorphic features, and intellectual disability: Diagnostic clues for α-thalassemia/mental retardation associated with chromosome 16 syndrome;Pediatrics & Neonatology;2022-05
3. ATR-16 syndrome: mechanisms linking monosomy to phenotype;Journal of Medical Genetics;2020-01-31
4. ATR16 Syndrome: Mechanisms Linking Monosomy to Phenotype;2019-10-07
5. Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility;Human Reproduction;2018-03-29
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