Correlation between testicular tissue and H-Y phenotype in intersex patients

Three-point multivariate calibration models by correlation constrained MCR-ALS: A feasibility study for quantitative analysis of complex mixtures.

Talanta·2016

Screening of patients with Turner syndrome for "hidden" Y-mosaicism.

Klinische Padiatrie·1999

Low insulin, IGF-I and IGFBP-3 levels in children with Prader-Labhart-Willi syndrome.

European journal of pediatrics·1998

Treatment with human growth hormone in patients with Prader-Labhart-Willi syndrome reduces body fat and increases muscle mass and physical performance.

European journal of pediatrics·1998

Timbral recognition and appraisal by adult cochlear implant users and normal-hearing adults.

Journal of the American Academy of Audiology·1998

Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndrome.

The Journal of urology·1997

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Clinical genetics·2026

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Clinical genetics·2026

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

Clinical genetics·2026

Enhancing Diagnostic Precision in Non-Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing-A Prospective Cohort Study.

Clinical genetics·2026

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures.

Clinical genetics·2026

A case of diffuse large B-cell lymphoma achieving complete remission with epcoritamab after pseudoprogression.

Journal of clinical and experimental hematopathology : JCEH·2026

Cytokine-associated ROS and Ca2+ dysregulation in severe inflammatory cardiomyopathy.

Cardiovascular research·2026

Acute EBV-Associated Systemic Inflammatory Syndrome Presenting as PUO With FDG-Avid Generalized Lymphadenopathy, Autoimmune Serological Positivity and Myopericarditis Mimicking Lymphoma and Connective Tissue Disease: A Diagnostic Challenge.

Cureus·2026

Gradually Enlarging Nodular Pulmonary Amyloidosis Associated With Sjögren's Syndrome.

Respirology case reports·2026

A Case of Thyroid Dermopathy.

Cureus·2026

Immune dysregulation in osteoarthritis: Mechanisms, biomarkers, and therapeutic opportunities.

Journal of translational autoimmunity·2026

Related Experiment Videos

Correlation between testicular tissue and H-Y phenotype in intersex patients

Related Concept Videos

Three-point multivariate calibration models by correlation constrained MCR-ALS: A feasibility study for quantitative analysis of complex mixtures.

Screening of patients with Turner syndrome for "hidden" Y-mosaicism.

Low insulin, IGF-I and IGFBP-3 levels in children with Prader-Labhart-Willi syndrome.

Treatment with human growth hormone in patients with Prader-Labhart-Willi syndrome reduces body fat and increases muscle mass and physical performance.

Timbral recognition and appraisal by adult cochlear implant users and normal-hearing adults.

Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndrome.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

Enhancing Diagnostic Precision in Non-Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing-A Prospective Cohort Study.

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures.

A case of diffuse large B-cell lymphoma achieving complete remission with epcoritamab after pseudoprogression.

Cytokine-associated ROS and Ca2+ dysregulation in severe inflammatory cardiomyopathy.

Acute EBV-Associated Systemic Inflammatory Syndrome Presenting as PUO With FDG-Avid Generalized Lymphadenopathy, Autoimmune Serological Positivity and Myopericarditis Mimicking Lymphoma and Connective Tissue Disease: A Diagnostic Challenge.

Gradually Enlarging Nodular Pulmonary Amyloidosis Associated With Sjögren's Syndrome.

A Case of Thyroid Dermopathy.

Immune dysregulation in osteoarthritis: Mechanisms, biomarkers, and therapeutic opportunities.

Related Experiment Videos

Correlation between testicular tissue and H-Y phenotype in intersex patients

Related Concept Videos

Related Articles