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Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes
WF. Blum, J. Klammt, S. Amselem, HM. Pfäffle, M. Legendre, ML. Sobrier, MP. Luton, CJ. Child, C. Jones, AG. Zimmermann, CA. Quigley, GB. Cutler, CL. Deal, J. Lebl, RG. Rosenfeld, JS. Parks, RW. Pfäffle,
Language English Country Netherlands
Document type Journal Article, Multicenter Study, Observational Study
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- MeSH
- Child MeSH
- Phenotype MeSH
- Homeodomain Proteins genetics MeSH
- Pituitary Gland growth & development metabolism MeSH
- Dwarfism, Pituitary genetics metabolism physiopathology MeSH
- Nuclear Proteins genetics MeSH
- Humans MeSH
- Human Growth Hormone genetics MeSH
- Adolescent MeSH
- Young Adult MeSH
- Mutation * MeSH
- DNA Mutational Analysis MeSH
- Child, Preschool MeSH
- Prospective Studies MeSH
- Zinc Finger Protein Gli2 genetics MeSH
- LIM-Homeodomain Proteins genetics MeSH
- Receptors, Pituitary Hormone-Regulating Hormone MeSH
- Receptors, Neuropeptide MeSH
- Transcription Factor Pit-1 genetics MeSH
- SOXB1 Transcription Factors genetics MeSH
- Transcription Factors genetics MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
Department of Pediatrics Oregon Health and Science University Portland USA
Eli Lilly and Company Indianapolis USA
Eli Lilly and Company Werner Reimers Strasse 2 4 61352 Bad Homburg Germany
Eli Lilly and Company Windlesham GU20 6PH UK
Gordon Cutler Consultancy LLC Deltaville USA
References provided by Crossref.org
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