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D chromosomes
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Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Mouse Phenotypes - Multiple malformation syndrome, moderate short stature, facial
Expression profiling in Williams-Beuren Syndrome patient fibroblast cell lines
Pluripotent cells derived from fibroblasts of patients with aberrant 7q11.23 dosage
Meningiomas with del(22q), del(1p36), or complex karyotypes associated with del(1p36) or del(14q)
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Staining and embedding of human chromosomes for 3-d serial block-face scanning electron microscopy.
Retention of D genome chromosomes in pentaploid wheat crosses.
A method to produce radiation hybrids for the D-genome chromosomes of wheat (Triticum aestivum L.).
Genetic fine mapping and candidate gene analysis of the Gossypium hirsutum Ligon lintless-1 (Li1) mu…
A recessive mutation causing oogenesis disruption found in the third chromosome of D. melanogaster s…
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Biomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo)
Genetic Markers in Patients With Colorectal Cancer
Pre-Implantation Genetic Screening in Women Under the Age of 36 Years With Single Embryo Transfer
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles
Turner Syndrome: Genotype and Phenotype
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