- Title
- Functional Characterization of a Heterozygous GLI2 Missense Mutation in Patients With Multiple Pituitary Hormone Deficiency
- Creators
- G. M. C Flemming - Hospital for Children and Adolescents (G.M.C.F., J.K., W.F.B., H.S., R.W.P.), University of Leipzig, D-04103 Leipzig, GermanyJ Klammt - Hospital for Children and Adolescents (G.M.C.F., J.K., W.F.B., H.S., R.W.P.), University of Leipzig, D-04103 Leipzig, GermanyG Ambler - The Children's Hospital at Westmead and University of Sydney (G.A., C.C., K.D., N.H.), Westmead, New South Wales 2145, AustraliaY Bao - Leonard Miller School of Medicine (Y.B., J.S.), University of Miami, Mailman Center for Child Development, Miami, Florida 33136W. F Blum - Hospital for Children and Adolescents (G.M.C.F., J.K., W.F.B., H.S., R.W.P.), University of Leipzig, D-04103 Leipzig, Germany, Lilly Research Laboratories (W.F.B.), Eli Lilly and Company, D-61352 Bad Homburg, GermanyC Cowell - The Children's Hospital at Westmead and University of Sydney (G.A., C.C., K.D., N.H.), Westmead, New South Wales 2145, AustraliaK Donaghue - The Children's Hospital at Westmead and University of Sydney (G.A., C.C., K.D., N.H.), Westmead, New South Wales 2145, AustraliaN Howard - The Children's Hospital at Westmead and University of Sydney (G.A., C.C., K.D., N.H.), Westmead, New South Wales 2145, AustraliaA Kumar - Virginia Commonwealth University Health System (A.K.), Richmond, Virginia 23298J Sanchez - Leonard Miller School of Medicine (Y.B., J.S.), University of Miami, Mailman Center for Child Development, Miami, Florida 33136H Stobbe - Hospital for Children and Adolescents (G.M.C.F., J.K., W.F.B., H.S., R.W.P.), University of Leipzig, D-04103 Leipzig, GermanyR. W Pfäffle - Hospital for Children and Adolescents (G.M.C.F., J.K., W.F.B., H.S., R.W.P.), University of Leipzig, D-04103 Leipzig, Germany
- Publication Details
- The journal of clinical endocrinology and metabolism, Vol.98(3), pp.E567-E575
- Academic Unit
- Miller School of Medicine; UMMG Department of Pediatrics; UMMG Dept of Pediatrics - Endocrinology
- Language
- English
- Resource Type
- Journal article
- PMID
- 23408573
- PMCID
- PMC3590478
- Record Identifier
- 991031576545102976
Journal article
Functional Characterization of a Heterozygous GLI2 Missense Mutation in Patients With Multiple Pituitary Hormone Deficiency
The journal of clinical endocrinology and metabolism, Vol.98(3), pp.E567-E575
2013-03-01
PMCID: PMC3590478
PMID: 23408573
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- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.108 Molecular & Cell Biology - Cancer & Development
- 1.108.1856 Hedgehog
- Web Of Science research areas
- Endocrinology & Metabolism
- ESI research areas
- Clinical Medicine
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Source: InCites