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21 results on '"Horike-Pyne, Martha"'

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

4. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

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

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

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

8. De novo variants in DENND5B cause a neurodevelopmental disorder

9. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

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

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

12. De novo variants in DENND5B cause a neurodevelopmental disorder

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

15. Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

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

17. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

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. Biallelic CRELD1variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

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