Patient with a deletion of chromosome 21q and minimal phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference9 articles.
1. Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation
2. Clonability and gene distribution on human chromosome 21: reflections of junk DNA content?
3. YAC analysis and minimal tiling path construction for chromosome 21q
4. Bacterial Contig Map of the 21q11 Region Associated with Alzheimer’s Disease and Abnormal Myelopoiesis in Down Syndrome
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature;Molecular Cytogenetics;2016-02-24
2. Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements;Molecular Cytogenetics;2016-01-28
3. Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient;Clinical Case Reports;2015-08-20
4. Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region;PLOS Genetics;2015-03-24
5. Modeling Partial Monosomy for Human Chromosome 21q11.2-q21.1 Reveals Haploinsufficient Genes Influencing Behavior and Fat Deposition;PLoS ONE;2012-01-20
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