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36 results on '"Weisz-Hubshman, Monika"'

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1. Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors

2. Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement

3. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

4. Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder

5. The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing

6. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

7. De novo variants in DENND5B cause a neurodevelopmental disorder

8. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

9. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

10. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

11. De novo variants in DENND5B cause a neurodevelopmental disorder

12. Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability

13. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

14. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

16. P428: De novo truncating variants in ZNF865: A putative cause of a neurodevelopmental disorder

18. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

19. Rare variants inPPFIA3cause delayed development, intellectual disability, autism, and epilepsy

22. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

24. Homozygous MED25 mutation implicated in eye–intellectual disability syndrome

27. Homozygous MED25 mutation implicated in eye-intellectual disability syndrome

28. Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability

30. A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder

31. Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa

32. Is one diagnosis the whole story? patients with double diagnoses

33. Homozygous MED25 mutation implicated in eye-intellectual disability syndrome

34. Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability.

35. Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy.

36. Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa.

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