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1. The Human Phenotype Ontology in 2024: phenotypes around the world

3. Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis

5. Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology

6. GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

8. Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome

11. An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome

12. Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia

13. Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences

14. First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders

15. Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances

16. An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype.

17. Mortality in Patients with 22q11.2 Rearrangements.

18. Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

19. Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosis

20. Mosaic Variegated Aneuploidy syndrome 2 caused by biallelic variants in CEP57, two new cases and review of the phenotype

22. Phenotypic spectrum and tumor risk in Simpson‐Golabi‐Behmel syndrome: Case series and comprehensive literature review.

23. Non‐immune hydrops fetalis is associated with bi‐allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene.

24. Deep Phenotyping and Genetic Characterization of a Cohort of 70 Individuals With 5p Minus Syndrome

26. Comprehensive Screening of Genetic Variants in the Coding Region of F8 in Severe Hemophilia A Reveals a Relationship with Disease Severity in a Colombian Cohort.

27. A Novel Missense Variant in the NKX2-1 Homeodomain Prevents Transcriptional Rescue by TAZ.

30. Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions

31. A six-attribute classification of genetic mosaicism

33. Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

34. The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome

35. NEOPLASIA ENDÓCRINA MÚLTIPLE Y ENFERMEDAD INFLAMATORIA INTESTINAL DE INICIO MUY TEMPRANO. UNA ASOCIACIÓN INESPERADA.

36. NGS Custom Panel Implementation in Patients with Non-Syndromic Autism Spectrum Disorders in the Clinical Routine of a Tertiary Hospital

37. The Human Phenotype Ontology in 2024: phenotypes around the world

38. Seven Additional Patients with SOX17 Related Pulmonary Arterial Hypertension and Review of the Literature

40. Lamb–Shaffer syndrome: 20 Spanish patients and literature review expands the view of neurodevelopmental disorders caused by SOX5 haploinsufficiency

41. In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype

44. Snijders Blok–Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review

47. HLA‐A*11:01 and HLA‐C*04:01 are associated with severe COVID‐19.

50. CLAPO syndrome: identification of somatic activating PIK3CA mutations and delineation of the natural history and phenotype

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