Found: 6
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WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 6, p. 1690, doi. 10.1002/ajmg.a.38206
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- Article
A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 11, p. 2849, doi. 10.1002/ajmg.a.35694
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- Article
The Vitamin D, IL-6 and the eGFR Markers a Possible Way to Elucidate the Lung–Heart–Kidney Cross-Talk in COVID-19 Disease: A Foregone Conclusion.
- Published in:
- Microorganisms, 2021, v. 9, n. 9, p. 1903, doi. 10.3390/microorganisms9091903
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- Article
Human Papillomavirus Carcinogenicity and the Need of New Perspectives: Thoughts from a Retrospective Analysis on Human Papillomavirus Outcomes Conducted at the Hospital University of Bari, Apulia, Italy, between 2011 and 2022.
- Published in:
- Diagnostics (2075-4418), 2024, v. 14, n. 9, p. 968, doi. 10.3390/diagnostics14090968
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- Article
Intragenic Deletion of the ZMYND11 Gene in 10p15.3 is Associated with Developmental Delay Phenotype: A Case Report.
- Published in:
- Cytogenetic & Genome Research, 2021, v. 161, n. 8/9, p. 445, doi. 10.1159/000518689
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- Article
Human Chondrocytes from Human Adipose Tissue-Derived Mesenchymal Stem Cells Seeded on a Dermal-Derived Collagen Matrix Sheet: Our Preliminary Results for a Ready to Go Biotechnological Cartilage Graft in Clinical Practice.
- Published in:
- Stem Cells International, 2021, p. 1, doi. 10.1155/2021/6664697
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- Article