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32 results on '"Roberto, Mendoza-Londono"'

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1. A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methods

4. O05: A micro-costing and cost-effectiveness analysis of genome sequencing vs exome sequencing in pediatric rare diseases

7. P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service

8. P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape

9. P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing

10. P873: 'If you look for a problem, you’ll find one': A qualitative study to understand why parents/adult patients decline secondary findings

11. A rare unbalanced translocation (trisomy 5q33.3‐qter, monosomy 13q34‐qter) results in growth hormone deficiency and brain anomalies

12. New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome

13. Severe Neonatal Cholestasis as an Early Presentation of McCune- Albright Syndrome

14. Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant

15. Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

16. A rare unbalanced translocation (trisomy 5q33.3‐qter, monosomy 13q34‐qter) results in growth hormone deficiency and brain anomalies

17. Do offers of admission to regional medical campuses impact an applicant's decision to decline their acceptance to medical school?

18. COG5 variants lead to complex early onset retinal degeneration, upregulation of PERK and DNA damage

19. DNA methylation signature for EZH2 functionally classifies sequence variants in three PRC2 complex genes

20. Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome

21. Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care

22. The 2017 international classification of the Ehlers-Danlos syndromes

23. Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders

24. De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia

25. Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

26. Severe intellectual disability and autistic features associated with microduplication 2q23.1

27. Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activity

28. Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes

29. X-linked retinoschisis in three females from the same family: A phenotype-genotype correlation

31. Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS

32. Prevalence of inherited neurotransmitter disorders in patients with movement disorders and epilepsy: a retrospective cohort study

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