Works matching IS 03406717 AND DT 2019 AND VI 138 AND IP 5
Results: 13
Special issue on canine genetics: animal models for human disease and gene therapies, new discoveries for canine inherited diseases, and standards and guidelines for clinical genetic testing for domestic dogs.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 437, doi. 10.1007/s00439-019-02025-5
- By:
- Publication type:
- Article
Personalized medicine: going to the dogs?
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 467, doi. 10.1007/s00439-019-02020-w
- By:
- Publication type:
- Article
Quality assurance checklist and additional considerations for canine clinical genetic testing laboratories: a follow-up to the published standards and guidelines.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 501, doi. 10.1007/s00439-019-02013-9
- By:
- Publication type:
- Article
Predicting copper toxicosis: relationship between the ATP7A and ATP7B gene mutations and hepatic copper quantification in dogs.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 541, doi. 10.1007/s00439-019-02010-y
- By:
- Publication type:
- Article
A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 535, doi. 10.1007/s00439-019-02005-9
- By:
- Publication type:
- Article
Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 455, doi. 10.1007/s00439-019-02003-x
- By:
- Publication type:
- Article
Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 441, doi. 10.1007/s00439-019-01999-6
- By:
- Publication type:
- Article
Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 525, doi. 10.1007/s00439-019-01997-8
- By:
- Publication type:
- Article
A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 509, doi. 10.1007/s00439-019-01986-x
- By:
- Publication type:
- Article
Correction to: Gene therapies in canine models for Duchenne muscular dystrophy.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Gene therapies in canine models for Duchenne muscular dystrophy.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 483, doi. 10.1007/s00439-019-01976-z
- By:
- Publication type:
- Article
A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 515, doi. 10.1007/s00439-019-01973-2
- By:
- Publication type:
- Article
Standards and guidelines for canine clinical genetic testing laboratories.
- Published in:
- Human Genetics, 2019, v. 138, n. 5, p. 493, doi. 10.1007/s00439-018-1954-4
- By:
- Publication type:
- Article