Article
Licensed
Unlicensed
Requires Authentication
Detection of Hidden Y Mosaicism in Turner's Syndrome: Importance in the Prevention of Gonadoblastoma
-
B. Bianco,
, M.V.N. Lipay, , M.I. Melaragno, , A.D. Guedes, and I.T.N. Verreschi,
Published/Copyright:
September 1, 2006
Published Online: 2006-09
©2011 by Walter de Gruyter GmbH & Co.
You are currently not able to access this content.
You are currently not able to access this content.
Articles in the same Issue
- TABLE OF CONTENTS
- Beyond the Karyotype: Are New Screening Methods Needed for Girls with Turner's Syndrome?
- The Treatment of Graves' Disease in Children
- Detection of Hidden Y Mosaicism in Turner's Syndrome: Importance in the Prevention of Gonadoblastoma
- Newborn Screening Levels of 17-Hydroxyprogesterone in Very Low Birth Weight Infants and the Relationship to Chronic Lung Disease
- Anabolic Steroid and Gonadotropin Releasing Hormone Analog Combined Treatment Increased Pubertal Height Gain and Adult Height in Two Children who Entered Puberty with Short Stature
- Relationships of IGF-I and Androgens to Skeletal Maturation in Obese Children and Adolescents
- Predictors of Metabolic Control at One Year in a Population of Pediatric Patients with Type 2 Diabetes Melttus: A Retrospective Study
- Serum Lipid Profile in Children Receiving Anti-epileptic Drug Monotherapy: Is it Atherogenic?
- Compound Heterozygosity of a Frameshift Mutation in the Coding Region and a Single Base Substitution in the Promoter of the ACTH Receptor Gene in a Family with Isolated Glucocorticoid Deficiency
- Novel Compound Heterozygous Mutation of the MC2R Gene in a Patient with Familial Glucocorticoid Deficiency
- Complex Urogenital Malformation Associated with Female Pseudohermaphroditism: Caudal Dysgenesis Syndrome
- Importance of Thyroglobulin Levels for Diagnosis and Monitoring of Follicular Thyroid Carcinoma in an Adolescent with Severe Iodine Deficiency
- Two Years of Growth Hormone Treatment in the First Growth Hormone Deficient Patient with Cerebrofaciothoracic Dysplasia
- CALENDAR
Articles in the same Issue
- TABLE OF CONTENTS
- Beyond the Karyotype: Are New Screening Methods Needed for Girls with Turner's Syndrome?
- The Treatment of Graves' Disease in Children
- Detection of Hidden Y Mosaicism in Turner's Syndrome: Importance in the Prevention of Gonadoblastoma
- Newborn Screening Levels of 17-Hydroxyprogesterone in Very Low Birth Weight Infants and the Relationship to Chronic Lung Disease
- Anabolic Steroid and Gonadotropin Releasing Hormone Analog Combined Treatment Increased Pubertal Height Gain and Adult Height in Two Children who Entered Puberty with Short Stature
- Relationships of IGF-I and Androgens to Skeletal Maturation in Obese Children and Adolescents
- Predictors of Metabolic Control at One Year in a Population of Pediatric Patients with Type 2 Diabetes Melttus: A Retrospective Study
- Serum Lipid Profile in Children Receiving Anti-epileptic Drug Monotherapy: Is it Atherogenic?
- Compound Heterozygosity of a Frameshift Mutation in the Coding Region and a Single Base Substitution in the Promoter of the ACTH Receptor Gene in a Family with Isolated Glucocorticoid Deficiency
- Novel Compound Heterozygous Mutation of the MC2R Gene in a Patient with Familial Glucocorticoid Deficiency
- Complex Urogenital Malformation Associated with Female Pseudohermaphroditism: Caudal Dysgenesis Syndrome
- Importance of Thyroglobulin Levels for Diagnosis and Monitoring of Follicular Thyroid Carcinoma in an Adolescent with Severe Iodine Deficiency
- Two Years of Growth Hormone Treatment in the First Growth Hormone Deficient Patient with Cerebrofaciothoracic Dysplasia
- CALENDAR