Disomy 21 in Spermatozoa and the Paternal Origin of Trisomy 21 Down Syndrome

Molecular Cytogenetics - United Kingdom
doi 10.1186/s13039-015-0155-2
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Paternal Uniparental Disomy of Chromosome 21

2020English

+21 or Trisomy 21

Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer ResearchOncologyGeneticsHematology
2011English

Down Syndrome: Characterisation of a Case With Partial Trisomy of Chromosome 21 Owing to a Paternal Balanced Translocation (15;21) (Q26;q22.1) by FISH.

Journal of Medical Genetics
Genetics
1997English

PCR-Based Detection of Parental Origin of Extra Chromosome 21 in Down Syndrome

International Journal of Human Genetics
Genetics
2005English

Trisomy 21 and Early Brain Development

Trends in Neurosciences
Neuroscience
2012English

Trisomy 21 and Facial Developmental Instability

American Journal of Physical Anthropology
AnatomyAnthropology
2013English

Trisomy 21 Represses Cilia Formation and Function

Developmental Cell
BiochemistryDevelopmental BiologyGeneticsCell BiologyMolecular Biology
2018English

Prognostic Impact of Trisomy 21 in Follicular Lymphoma

British Journal of Haematology
Hematology
2018English

A Non-Mosaic Humanized Mouse Model of Down Syndrome, Trisomy of the Long Arm of Human Chromosome 21 in Mouse Chromosome Background

2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy