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

Childhood monosomy 7: epidemiology, biology, and mechanistic implications.

Blood - 15 Apr 1995

Luna-Fineman S, Shannon K M, Lange B J

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 Chromosome Disorders
Share to Chromosomes, Human, Pair 7
Share to Genes, Neurofibromatosis 1
Share to Hematopoietic Stem Cells

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid

Share to Monosomy

Share to Myelodysplastic Syndromes

Share to Neoplasms, Second Primary

Source

Identifiers

PMID: 7718870

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Childhood monosomy 7: epidemiology, biology, and mechanistic implications.PMID 7718870Read ↗

Additional studies warranted to confirm monosomy 21Semantic proximity Read ↗

Trisomy in humans: incidence, origin and etiologySemantic proximity Read ↗

Monosomy 7 in Pediatric Myelodysplastic SyndromesSemantic proximity Read ↗

Broadening our understanding by the use of molecular cytogenetic techniques: full monosomy 21.Semantic proximity Read ↗

Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.Semantic proximity Read ↗

The enigma of monosomy 7Semantic proximity Read ↗

Bibliography. Current world literature. Pediatric and heritable disorders.Semantic proximity Read ↗

Bibliography. Current world literature. Pediatric and heritable disorders.Semantic proximity Read ↗

Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7Semantic proximity Read ↗

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of PhiladelphiaSemantic proximity Read ↗

American College of Medical Genetics Statement on Diagnostic Testing for Uniparental DisomySemantic proximity Read ↗

Fifty years of recognizable patterns of human malformation: Insights and opportunities.Semantic proximity Read ↗

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