Genetic disorders in adolescents and young adults

The prenatal detection of the fragile X chromosome: review of recent experience.

American journal of medical genetics·1986

Evidence for genetic control of nondisjunction in man.

American journal of human genetics·1980

Chromosome fragility and susceptibility of Bloom's syndrome fibroblasts to SV40 transformation.

Experientia·1980

Medical genetics for the otorhinolaryngologist.

The Laryngoscope·1980

Correlation between prognosis and bone marrow chromosomal patterns in children with acute nonlymphocytic leukemia: similarities and differences compared to adults.

Blood·1979

Ocular findings in cytogenetic syndromes.

Ophthalmology·1979

No Child Left Behind: Advancing Access in Pediatric Dermatology, a 4-Year, Single-Center Experience.

Pediatric clinics of North America·2026

Telemedicine and Access to Pediatric Dermatology Care.

Pediatric clinics of North America·2026

Inequitable Reimbursement for Pediatric Providers: A Review of Structural Factors that Disincentivize the Care of Children.

Pediatric clinics of North America·2026

Medical Photography's Power to Change Medical Care.

Pediatric clinics of North America·2026

Insurance Hurdles for Laser Authorization in Pediatric Patients.

Pediatric clinics of North America·2026

Controversies in Increasing the Pipeline for Pediatric Dermatology.

Pediatric clinics of North America·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

Genetic disorders in adolescents and young adults

Related Concept Videos

The prenatal detection of the fragile X chromosome: review of recent experience.

Evidence for genetic control of nondisjunction in man.

Chromosome fragility and susceptibility of Bloom's syndrome fibroblasts to SV40 transformation.

Medical genetics for the otorhinolaryngologist.

Correlation between prognosis and bone marrow chromosomal patterns in children with acute nonlymphocytic leukemia: similarities and differences compared to adults.

Ocular findings in cytogenetic syndromes.

No Child Left Behind: Advancing Access in Pediatric Dermatology, a 4-Year, Single-Center Experience.

Telemedicine and Access to Pediatric Dermatology Care.

Inequitable Reimbursement for Pediatric Providers: A Review of Structural Factors that Disincentivize the Care of Children.

Medical Photography's Power to Change Medical Care.

Insurance Hurdles for Laser Authorization in Pediatric Patients.

Controversies in Increasing the Pipeline for Pediatric Dermatology.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Related Experiment Videos

Genetic disorders in adolescents and young adults

Related Concept Videos

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