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XX gonadal dysgenesis
Genetic Disorders in Premature Ovarian Failure
Turner Syndrome Diagnosed in Northeastern Malaysia Kannan T P, Azman B Z, Ahmad Tarmizi a B, Suhaida M A, Siti Mariam I, Ravindran A, Zilfalil B A
Orphanet Report Series Rare Diseases Collection
Intersex 101
From Gene to Gender - What We’Ve Learned and What We Need to Learn - New Prospects in DSD Research
Redalyc.An Approach to the Biological, Historical and Psychological
Endocrine Test Selection and Interpretation
'Control of Sex Development'
Down Syndrome from Wikipedia, the Free Encyclopedia Jump To: Navigation, Search
Adolescent Girls with Pure Gonadal Dysgenesis: a Rare Disease J Sahaa, K Begumb, KA Khanomc, I Prasadd, S Aktere
Endocrinology
Genetic Aspects of Premature Ovarian Failure Wieacker P J
Gene Analysis in Patients with Premature Ovarian Failure Or
Comparison of Adult Height Between Patients J Med Genet: First Published As 10.1136/Jmg.29.8.539 on 1 August 1992
46, XX Male, 46, XY Female and 46, XX- 46XY Female Variants: Rare Stories We Must Consider in the Assessment of the Disorder of Sex Development
Clinical and Genetic Aspects of Mayer–Rokitansky–Küster– Hauser Syndrome
New NR5A1 Mutations and Phenotypic Variations of Gonadal Dysgenesis
Not All Growth Disorders Reflect Hormone Deficit
Top View
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Cytogenetic Evaluation of Patients with Clinical Spectrum of Turner Syndrome
Misdiagnosis of Mullerian Agenesis in a Patient with 46, XX Gonadal Dysgenesis: a Missed Opportunity for Prevention of Osteoporosis
List Rare Diseases.Txt
Applying Forward Genetic Approaches to Rare Mendelian
Intersex: Stories and Statistics from Australia
Two Males with SRY-Positive 46,XX Testicular Disorder of Sex Development
Peptide Hormone Analysis in Diagnosis and Treatment of Differences
Health and Wellbeing of People with Intersex Variations Information and Resource Paper
An Overview on the Genetic Determinants of Infertility
SBB3101 Subject Name: Medical Biotechnology Subject Code: SBB3101
Sex Determination Secondary Article
11B-Hydroxylase Deficiency, 36 17,20 Desmolase Deficiency, 36 17
A Case of Premature Ovarian Failure in a 33-Year-Old Woman
Premature Ovarian Insufficiency Precision Panel Overview Indications
Y Genes: Unraveling the Molecular Pathogenesis of Disorders of Sex Development
Prevalence and Incidence of Rare Diseases
Gonadal Dysgenesis Precision Panel Overview Indications Clinical Utility
List of Rare Diseases and Synonyms
Primary Gonadal Failure
Disorders of Gonadal Development in Humans
Orphanet Report Series Rare Diseases Collection
Küster-Hauser Syndrome
Premature Ovarian Failure) - Uptodate