Document Detail

New variant of chromosome 11.
MedLine Citation:
PMID:  8042675     Owner:  NLM     Status:  MEDLINE    
An additional C-positive band in the centromeric region (p11) was observed in a man. By GTG- and RBA-techniques it was positively stained but by QFQ-technique the staining intensity was negative. Although he was identified through fetal loss in his wife, it apparently represents a familial variant whose clinical significance is unknown.
V Aiello; N Ricci; P Palazzi; G D'Agostino; G Azzini; E Calzolari
Related Documents :
70995 - Frequency of satellite association of human chromosomes is correlated with amount of ag...
21701565 - A genome-wide association study of bmi in american indians.
25373145 - Megabase-scale deletion using crispr/cas9 to generate a fully haploid human cell line.
21537955 - The in vitro mn assay in 2011: origin and fate, biological significance, protocols, hig...
16971405 - Genetic determinants of c-reactive protein in copd.
14871365 - Phylogeographical patterns of genetic divergence and speciation in african mole-rats (f...
Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  American journal of medical genetics     Volume:  50     ISSN:  0148-7299     ISO Abbreviation:  Am. J. Med. Genet.     Publication Date:  1994 Apr 
Date Detail:
Created Date:  1994-08-24     Completed Date:  1994-08-24     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7708900     Medline TA:  Am J Med Genet     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  294-5     Citation Subset:  IM    
Istituto di Genetica Medica, Università degli Studi di Ferrara, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Abortion, Habitual
Centromere / ultrastructure
Chromosome Aberrations / genetics*
Chromosome Banding
Chromosome Disorders
Chromosomes, Human, Pair 11 / ultrastructure*
Y Chromosome / ultrastructure

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Child with Sotos phenotype and a 5:15 translocation.
Next Document:  Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.