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45 results on '"Hammarsjö, Anna"'

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1. Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon

2. Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13

4. Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

5. Compound heterozygosity for two variants in BMP5 in human skeletal dysostosis with atrioventricular septal defect.

6. Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant

7. High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses

8. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

10. Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome

11. Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders

12. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

13. Compound heterozygous variants in RAB34 in a rare skeletal ciliopathy syndrome.

14. Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability

16. A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay

18. Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability

19. A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

20. Case report: Extending the spectrumof clinical andmolecular ?ndings in FOXC1 haploinsufficiency syndrome.

21. Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders.

24. Additional file 1 of Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

25. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

26. Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non‐oncologic disorders

27. Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders

28. Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome

30. Gain-of-function mutation of microRNA-140 in human skeletal dysplasia

31. Expanding the genetic and phenotypic spectrum of skeletal dysplasias

32. A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation

33. Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias

35. Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2

37. Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in <italic>PLOD2</italic>.

39. A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach–Nishimura skeletal dysplasia due to pathogenic variants in ALG9

43. A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach–Nishimura skeletal dysplasia due to pathogenic variants in ALG9

44. GSTM1 Gene Expression Correlates to Leiomyoma Volume Regression in Response to Mifepristone Treatment.

45. A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay.

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