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1. The sixth international RASopathies symposium: Precision medicine-From promise to practice.

6. List of contributors

10. Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

21. Consultagene: Pre- and Post-Pandemic Experience with a Web-based Platform and Remote Delivery of Genetic Services

25. The sixth international RASopathies symposium : Precision medicine—From promise to practice

26. The sixth international RASopathies symposium: Precision medicine—From promise to practice

27. The sixth international RASopathies symposium: Precision medicine—From promise to practice

28. Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum

30. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide

31. Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants inNONO

32. Phenotypic expansion in DDX3X – a common cause of intellectual disability in females.

36. Corrigendum to “DNA Sequence Analysis of GJB2, Encoding Connexin 26: Observations From a Population of Hearing Impaired Cases and Variable Carrier Rates, Complex Genotypes, and Ethnic Stratification of Alleles Among Controls” Am J Med Genet Part A 140A:2401–2415

37. 601: Rapid prenatal diagnosis of cytogenetic abnormalities by array CGH analysis

39. DNA sequence analysis and genotype-phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy.

40. DNA sequence analysis ofGJB2, encoding connexin 26: Observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls

41. Hereditary Multiple Exostosis and Pain

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