The causes of mental retardation

The challenge of "Healthy People 2000".

Journal of genetic counseling·2013

RP463: a stabilized technetium-99m complex of a hydrazino nicotinamide derivatized chemotactic peptide for infection imaging.

Bioconjugate chemistry·1999

Biological evaluation of thrombus imaging agents utilizing water soluble phosphines and tricine as coligands when used to label a hydrazinonicotinamide-modified cyclic glycoprotein IIb/IIIa receptor antagonist with 99mTc.

Bioconjugate chemistry·1997

Data collection for the evaluation of mental retardation prevention activities: the fateful forty-three.

Mental retardation·1992

Head circumference of children with Down syndrome (0-36 months)

American journal of medical genetics·1992

Perceived needs of families with children who have chronic health conditions.

Children's health care : journal of the Association for the Care of Children's Health·1990

Centering Lived Experience: Inclusive Pediatric Care for Children Who Are Deaf and Hard of Hearing and Their Families.

Pediatric annals·2026

From Early Childhood to Adulthood: Implementing Neuroaffirming Health Care for Autistic Individuals.

Pediatric annals·2026

Neurodivergence in Medical Education: Current Landscape and Inclusive Future for Pediatrics.

Pediatric annals·2026

Neurodiversity and Intellectual Disability: Opportunities and Challenges for Functioning and Participation Across the Life Course.

Pediatric annals·2026

Action for Access: Equity for Children With Disabilities in Lowand Middle-Income Countries.

Pediatric annals·2026

Navigating Pediatric Urticaria: Diagnosis and Management for the Busy Pediatrician.

Pediatric annals·2026

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Cureus·2026

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Molecular syndromology·2026

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

Journal of immunology (Baltimore, Md. : 1950)·2026

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Arquivos de neuro-psiquiatria·2026

Expanding the clinical and molecular spectrum of SETD5, NEDD4L, and TBL1X related disorders: A case report and literature review.

Gene·2026

Developmental Profiles Associated with TUBA1A, TUBB2A, TUBB2B, and TUBB3 Tubulinopathy Conditions.

American journal on intellectual and developmental disabilities·2026

Related Experiment Videos

The causes of mental retardation

Related Concept Videos

The challenge of "Healthy People 2000".

RP463: a stabilized technetium-99m complex of a hydrazino nicotinamide derivatized chemotactic peptide for infection imaging.

Biological evaluation of thrombus imaging agents utilizing water soluble phosphines and tricine as coligands when used to label a hydrazinonicotinamide-modified cyclic glycoprotein IIb/IIIa receptor antagonist with 99mTc.

Data collection for the evaluation of mental retardation prevention activities: the fateful forty-three.

Head circumference of children with Down syndrome (0-36 months)

Perceived needs of families with children who have chronic health conditions.

Centering Lived Experience: Inclusive Pediatric Care for Children Who Are Deaf and Hard of Hearing and Their Families.

From Early Childhood to Adulthood: Implementing Neuroaffirming Health Care for Autistic Individuals.

Neurodivergence in Medical Education: Current Landscape and Inclusive Future for Pediatrics.

Neurodiversity and Intellectual Disability: Opportunities and Challenges for Functioning and Participation Across the Life Course.

Action for Access: Equity for Children With Disabilities in Lowand Middle-Income Countries.

Navigating Pediatric Urticaria: Diagnosis and Management for the Busy Pediatrician.

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Expanding the clinical and molecular spectrum of SETD5, NEDD4L, and TBL1X related disorders: A case report and literature review.

Developmental Profiles Associated with TUBA1A, TUBB2A, TUBB2B, and TUBB3 Tubulinopathy Conditions.

Related Experiment Videos

The causes of mental retardation

Related Concept Videos

Related Articles