Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization

A novel mutation of the fibrillin-1 gene in a newborn with severe Marfan syndrome.

Journal of perinatology : official journal of the California Perinatal Association·2008

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.

Annals of human genetics·2001

Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14.

Circulation·2001

HER-2/neu gene amplification in stages I-IV breast cancer detected by fluorescent in situ hybridization.

Genetics in medicine : official journal of the American College of Medical Genetics·2001

Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.

American journal of medical genetics·2000

Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.

Experimental and molecular pathology·2000

Child Opportunity Index: Paradoxical Risk of Pediatric Long COVID Cases.

Clinical pediatrics·2026

Oropharyngeal Gonorrhea and Chlamydia Testing in the Pediatric Emergency Department.

Clinical pediatrics·2026

Telehealth in Pediatrics: A Quick Review.

Clinical pediatrics·2026

The Doctor Will Zoom You Now: An Experiential Telemedicine Assessment for Pediatric Residents.

Clinical pediatrics·2026

Sleep Health in School-Aged Children: A Qualitative Study of Community-Based Pediatric Providers' Perspectives and Practices.

Clinical pediatrics·2026

Giardia duodenalis Infection and Pachymeningitis in a Patient With Agammaglobulinemia.

Clinical pediatrics·2026

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

International journal of legal medicine·2026

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

Phlebology·2026

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cytogenetic and genome research·2026

Cognitive flexibility deficits differ between the sexes in a transchromosomic mouse model of Down syndrome.

Disease models & mechanisms·2026

Compromised striatal structure and function in mouse models of RARB-related disorder.

Brain : a journal of neurology·2026

Defective neuronal differentiation in Lowe syndrome is associated with mitochondrial dysfunction and impaired cilia-related Sonic Hedgehog signaling.

eLife·2026

Related Experiment Videos

Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ

Related Concept Videos

A novel mutation of the fibrillin-1 gene in a newborn with severe Marfan syndrome.

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.

Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14.

HER-2/neu gene amplification in stages I-IV breast cancer detected by fluorescent in situ hybridization.

Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.

Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.

Child Opportunity Index: Paradoxical Risk of Pediatric Long COVID Cases.

Oropharyngeal Gonorrhea and Chlamydia Testing in the Pediatric Emergency Department.

Telehealth in Pediatrics: A Quick Review.

The Doctor Will Zoom You Now: An Experiential Telemedicine Assessment for Pediatric Residents.

Sleep Health in School-Aged Children: A Qualitative Study of Community-Based Pediatric Providers' Perspectives and Practices.

Giardia duodenalis Infection and Pachymeningitis in a Patient With Agammaglobulinemia.

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cognitive flexibility deficits differ between the sexes in a transchromosomic mouse model of Down syndrome.

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Related Experiment Videos

Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ...

Related Concept Videos

Related Articles

Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ