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Your search keyword '"Davis, Joie"' showing total 32 results

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32 results on '"Davis, Joie"'

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

2. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

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

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

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

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

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

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

11. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

12. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

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

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

15. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

16. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

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

18. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

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

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

21. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

22. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

23. Variants in PRKAR1Bcause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

24. Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

25. An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

26. Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency

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

30. The Stickler syndrome: Genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1

32. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

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