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1. Performance of Massive Parallel Sequencing-Based Cell-Free DNA Testing in Compromised Pregnancies.

6. ZDHHC15as a candidate gene for autism spectrum disorder

7. 16q12.2q21 deletion: A newly recognized cause of dystonia related to GNAO1 haploinsufficiency

8. A Novel Intragenic Duplication in the HDAC8 Gene Underlying a Case of Cornelia de Lange Syndrome

10. ZDHHC15 as a candidate gene for autism spectrum disorder.

14. Genomic Chaos (Multiple Copy Number Variations and Structural Reorganization) Detected in Two Prenatal Cases

19. Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8‐year long observational study from a tertiary care university hospital

20. Front Cover

21. Molecular characterization of Spanish patients withMECP2duplication syndrome

27. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy

28. Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8‐year long observational study from a tertiary care university hospital.

29. Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure

30. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy

33. PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome

35. Intrachromosomal 3p Insertion as a Cause of Reciprocal Pure Interstitial Deletion and Duplication in Two Siblings: Further Delineation of the Emerging Proximal 3p Deletion Syndrome

37. A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region

45. Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

49. Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

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