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Your search keyword '"Mulvihill, John J."' showing total 16 results

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16 results on '"Mulvihill, John J."'

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

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

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

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

7. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

10. De novo variants in DENND5B cause a neurodevelopmental disorder

11. Microindentation of fresh soft biological tissue: A rapid tissue sectioning and mounting protocol

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

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

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

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

16. Characterization of primary human leptomeningeal cells in 2D culture.

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