Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Double trisomy with 48, XXX+21 karyotype in a Down's syndrome child from Jammu and Kashmir, India.

Journal of genetics - 1 Dec 2008

Balwan Wahied Khawar, Kumar Parvinder, Raina T R, Gupta Subash

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Chromosomes, Human
Share to Down Syndrome
Share to India

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Karyotyping

Share to Phenotype

Share to Trisomy

Source

Identifiers

PMID: 19147910
DOI: 10.1007/s12041-008-0039-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Double trisomy with 48, XXX+21 karyotype in a Down's syndrome child from Jammu and Kashmir, India.PMID 19147910Read ↗

Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation.Semantic proximity Read ↗

Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotype.Semantic proximity Read ↗

A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome.Semantic proximity Read ↗

Nondisjunction in Trisomy 21: Origin and MechanismsSemantic proximity Read ↗

A male case with double aneuploidy (48,XXY,+21).Semantic proximity Read ↗

Chromosome 21 Disomy in the Spermatozoa of the Fathers of Children with Trisomy 21, in a Population with a High Prevalence of Down Syndrome: Increased Incidence in Cases of Paternal OriginSemantic proximity Read ↗

The prevalence and patterns of chromosome abnormalities in newborns with major congenital anomalies: A retrospective study from Saudi ArabiaSemantic proximity Read ↗

Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted?Semantic proximity Read ↗

Partial trisomy of chromosome 21 without the Down syndrome phenotype.Semantic proximity Read ↗

Cytogenetic and epidemiological findings in Down syndrome: England and Wales 1989–2009Semantic proximity Read ↗

Down-Klinefelter syndrome (48,XXY,+21) in a child with congenital heart disease: case report and literature review.Semantic proximity Read ↗

Chromosome 21 and Down syndrome: the post-sequence era.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.