Rare Diseases
Records 1 - 10 (of 10 Records) |
Query Trace: Microcephaly[original query]>>Reviews/Commentaries[Product Type] |
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Rare CNVs and Known Genes Linked to Macrocephaly: Review of Genomic Loci and Promising Candidate Genes. Bastos Giovanna Civitate et al. Genes 2022 13(12) |
Pitfalls in Genetic Testing for Consanguineous Pediatric Populations. Saleh Maha et al. Case reports in genetics 2022 20229393042 |
Molecular Genetics of Microcephaly Primary Hereditary: An Overview. Siskos Nikistratos et al. Brain sciences 2021 11(5) |
Zika Birth Defects Surveillance CDC, 2019 |
Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research. Innes A Micheil et al. American journal of medical genetics. Part C, Seminars in medical genetics 2018 Dec 178(4) 387-397 |
Identical Twins Hint at How Environments Change Gene Expression Studying twins has long offered insight into the interplay of nature and nurture. Epigenetics is the next frontier. E Hayasaki, The Atlantic, May 2018 |
The genetics of congenitally small brains. Duerinckx Sarah et al. Seminars in cell & developmental biology 2017 Sep |
Microcephaly: A clinical genetics approach G Woods, Up to Date 2015 |
Molecular genetics of human primary microcephaly: an overview. Faheem Muhammad, et al. BMC medical genomics 2015 0 0. S4 |
Genetic disorders associated with postnatal microcephaly. Seltzer Laurie E et al. American journal of medical genetics. Part C, Seminars in medical genetics 2014 Jun (2) 140-55 |