Hochschulschrift
Diagnosis and characterization of leptin mutations causing severe early-onset obesity
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
-
30 cm
- Extent
-
iv, 114 Blätter
- Language
-
Englisch
- Notes
-
Illustrationen, Diagramme
Universität Ulm, Dissertation, 2018
- Keyword
-
Fettsucht
Leptine
- Event
-
Veröffentlichung
- (where)
-
Ulm
- (when)
-
[2018]
- Creator
- Contributor
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.06.2025, 2:23 PM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
Time of origin
- [2018]
Other Objects (12)
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters
TERT Core Promotor Mutations in Early-Onset Bladder Cancer
Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB
Early-Onset Osteoporosis
BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients
Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations
Association between HLA-A gene polymorphism and early-onset preeclampsia in Chinese pregnant women early-onset
BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation
Novel mutations in the BRCA1 and BRCA2genes in Iranian women with early-onset breast cancer
Early-onset diabetes: an epidemic in China
Early-onset hereditary spastic paraplegia: case report
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters
TERT Core Promotor Mutations in Early-Onset Bladder Cancer
Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB
Early-Onset Osteoporosis
BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients
Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations
Association between HLA-A gene polymorphism and early-onset preeclampsia in Chinese pregnant women early-onset
BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation
Novel mutations in the BRCA1 and BRCA2genes in Iranian women with early-onset breast cancer
Early-onset diabetes: an epidemic in China
Early-onset hereditary spastic paraplegia: case report
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters
TERT Core Promotor Mutations in Early-Onset Bladder Cancer
Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB
Early-Onset Osteoporosis
BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients
Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations
Association between HLA-A gene polymorphism and early-onset preeclampsia in Chinese pregnant women early-onset
BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation
Novel mutations in the BRCA1 and BRCA2genes in Iranian women with early-onset breast cancer
Early-onset diabetes: an epidemic in China