Ring Chromosomes from Patients’ Perspective
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-47530-6_30
Reference5 articles.
1. Liehr T (2012) Small supernumerary marker chromosomes (sSMC): A guide for human geneticists and clinicians; with contributions by UNIQUE (The Rare Chromosome Disorder Support Group) Springer, Berlin
2. Liehr T (2014) Uniparental disomy (UPD) in clinical genetics. A guide for clinicians and patients. Springer, Berlin
3. Liehr T, Harutyunyan T, Williams H, Weise A (2022) Restrictions and advantages of non-invasive prenatal testing (NIPT). Scholar Community Encylopedia. https://encyclopedia.pub/entry/38834
4. Schaflinger E, Enko D (2022) Die Bedeutung der Hochdurchsatz-Sequenzierung in der medizinisch genetischen Diagnostik und Beratung [The impact of next-generation sequencing on medical genetic diagnostics and counseling]. Dtsch Med Wochenschr 147:1336–1341. https://doi.org/10.1055/a-1924-6646
5. Szczepura A, Wynn S, Searle B, Khan AJ, Palmer T, Biggerstaff D, Elliott J, Hultén MA (2018) UK families with children with rare chromosome disorders: Changing experiences of diagnosis and counselling (2003–2013). Clin Genet 93:972–981. https://doi.org/10.1111/cge.13207
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