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Your search keyword '"Palmer, Christina G.S."' showing total 30 results

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30 results on '"Palmer, Christina G.S."'

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

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

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

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

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

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

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

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

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

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

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

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

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

14. One is the loneliest number: genotypic matchmaking using the electronic health record

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

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

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

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

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

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

21. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

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

23. Evidence synthesis and guideline development in genomic medicine: current status and future prospects

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

26. Infant hearing loss and connexin testing in a diverse population

29. Evidence synthesis and guideline development in genomic medicine: current status and future prospects

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

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