20 results on '"Goksen, Damla"'
Search Results
2. Evaluation of the Frequency of Multiple Hormone Deficiency and Long-Term Data in Patients with Craniopharyngioma
3. Detection of Copy Number Variations by Microarray in Disorders of Sex Development of Unexplained Molecular Etiology and Association with Clinical Findings
4. Genetic causes of combined pituitary hormone deficiency
5. Crooke Cell Adenoma as a Rare Cause of Recurrent Cushing Disease: A Challenge in Treatment and Follow-Up
6. Molecular Genetic Diagnosis and Research of Candidate Genes by Targeted Next Generation Sequence Analysis and Whole Exome Sequencing Method in Monogenic Diabetes: MODY-TURK Project
7. The Molecular Genetic Etiology by Whole Exome Sequence Analysis in Cases With Familial Type 1 Diabetes Mellitus without HLA Haplotype Predisposition or Incomplete Predisposition
8. Plasma steroid panel with liquid chromotographymass spectrometry (LC/MS-MS) method: utilization in differential diagnosis of hyperandrogenism
9. Investigation of The Molecular Genetic Causes Of Non-Syndromic Premature Ovarian Failure By Next Generation Sequence Analysis
10. A case of gender developmental disorder with difficulty in molecular diagnosis: new variant in NR5A1 gene
11. Targeted Molecular Genetic Diagnosis by Next Generation Sequence Analysis Method and Investigation of Responsible Candidate Genes in Patients with Osteogenesis Imperfecta
12. Clinical and Molecular Spectrum of Patients with Disorders of Sex Development: A Single Center Experience
13. Clinical characteristics and response to growth hormone treatment in patients with Prader-Willi Syndrome
14. Gonadal Insufficiency and Affecting Factors in Patients with Bone MarrowTransplantation(BMT) for Non-malignantIndications in Childhood or Adolescence
15. Nationwide Hypophosphatemic Rickets Study
16. EXOME RESULTS IN UNDIAGNOSED 46, XY DISORDER OF SEX DEVELOPMENT CASES WITH TARGETED NEXT-GENERATION SEQUENCING
17. Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia: A Novel AMH Receptor Mutation
18. Prevalence of Melanocortin 4 Receptor Mutations in Turkish Obese Children
19. Precocious puberty in a patient with X linked adrenal Hypoplasia congenita due to DAX 1 mutation
20. Gonadotropin-dependent precocious puberty in a patient with X-linked adrenal hypoplasia congenita caused by a novel DAX-1 mutation.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.