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28 results on '"Jean-Marie, Orpa"'

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1. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

2. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

3. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

4. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

5. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

6. De novo variants in DENND5B cause a neurodevelopmental disorder

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

8. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

9. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

10. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

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

12. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

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

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

15. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

16. De novo variants in DENND5B cause a neurodevelopmental disorder

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

18. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

19. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

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

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

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

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

25. Loss-of-function in RBBP5results in a syndromic neurodevelopmental disorder associated with microcephaly

26. Dominant missense variants in SREBF2are associated with complex dermatological, neurological, and skeletal abnormalities

27. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

28. De novo variants in MRTFBhave gain-of-function activity in Drosophilaand are associated with a novel neurodevelopmental phenotype with dysmorphic features

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