- Home
- » Tags
- » Kallmann syndrome
Top View
- A Case of Kallmann Syndrome Associated with a Non-Functional Pituitary Microadenoma
- Neuroendocrinology of Reproduction 19 REGULATION of Gnrh RELEASE from Gnrh NEURONAL CELL LINES
- Kallmann's Syndrome: Clues to Clinical Diagnosis
- Genes Covered and Disorders Detected by X-HR Microarray
- Blueprint Genetics Kallmann Syndrome Panel
- Unique Phenotype in a Patient with CHARGE Syndrome
- Delayed Puberty
- Kallmann Syndrome Precision Panel Overview Indications
- Whole Genome Analysis As a Tool for Diagnosis in Silver-Russell
- Kidneyseq™: a Comprehensive Inherited Kidney Disease Panel Iowa Institute of Human Genetics
- Syndromic and Nonsyndromic Systemic Associations of Congenital Lacrimal Drainage Anomalies: a Major Review
- Kallman Syndrome (KAL1) Sequencing
- Diagnostic Findings in 60 Cases of Isolated and Syndromic Congenital
- Not All Growth Disorders Reflect Hormone Deficit
- Monogenic and Syndromic Obesity Precision Panel Overview Indications Clinical Utility
- PERSPECTIVE Genetic Causes of Human Reproductive Disease
- Kallmann Syndrome
- Review Article a Gene Map of Congenitalmalformations
- ORPHA Number Disease Or Group of Diseases 300305 11P15.4
- Kallmann Syndrome: a Case Report Pangastuti Nuring, Nisa Khairun, and Widad Shofwal Department of Obstetrics and Gynecology, Dr
- Pediatric Endocrinology
- Biennial Report on the Rare Diseases Research Activities at the National Institutes of Health FY 2006
- Case Report a Case of Male Osteoporosis: a 37-Year-Old Man with Multiple Vertebral Compression Fractures
- Blueprint Genetics Waardenburg Syndrome Panel
- Kallmann Syndrome: MR Evaluation of Olfactory System
- Rare Disease Impact Report: Insights from Patients and the Medical Community
- British Columbia Laboratory Requisition This Requisition Form, When Completed, Constitutes a Referral to Lifelabs/BC Biomedical Laboratories Physicians
- Genetics of Hypogonadotropic Hypogonadism
- Congenital Hypogonadotropic Hypogonadism/ Kallmann Syndrome Is Associated with Statural Gain in Both Men and Women: a Monocentric Study
- A Novel SOX10 Nonsense Mutation in a Patient with Kallmann Syndrome and Waardenburg Syndrome
- A Novel SOX10 Variant in a Japanese Girl with Waardenburg Syndrome
- Clinical, Endocrinological, and Molecular Characterization of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: a Single Center Experience
- Biology of Human Melanocyte Development, Piebaldism, and Waardenburg Syndrome
- The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis
- Head and Neck MRI Findings in CHARGE Syndrome
- Kallmann Syndrome: MR Findings
- Male Hypogonadism. Part II: Etiology, Pathophysiology, and Diagnosis
- An Update in the Genetic Aetiologies of Combined Pituitary Hormone Deficiency
- De Novo SOX10 Nonsense Mutation in a Patient with Kallmann Syndrome, Deafness, Iris Hypopigmentation, and Hyperthyroidism
- Laboratory Newsletter | Summer 2014 UNMC Human Genetics Laboratory
- Download Gene List
- Kallmann Syndrome
- Leistungsverzeichnis Der Sektion Pädiatrische Genetik Der Universitätskinderklinik Freiburg, Mathildenstr
- Prevalence and Incidence of Rare Diseases
- Kallmann's Syndrome: a Rare Cause of Primary Amenorrhoea
- Kallmann Syndromes MR Findings
- Short Stature Precision Panel Overview Indications Clinical Utility
- Differential Diagnosis and Genetic Testing for Determining the Molecular Causes Underlying Oro-Dental Anomalies in a Series of Patients
- List of Nephropathy Genes