Related Experiment Videos

Double supernumerary isochromosome 9p in myeloproliferative syndrome

J J Hoo¹, S O'Brien, I Samuel

¹Department of Pediatrics, University of Illinois at Chicago 60612.

Cancer Genetics and Cytogenetics

|December 1, 1987

Abstract:

The presence of supernumerary isochromosome 9p in duplicate in about 50% of bone marrow cells of an elderly female patient with myeloproliferative syndrome is reported.

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

First-trimester markers of aneuploidy in women positive for HIV.

BJOG : an international journal of obstetrics and gynaecology·2010

Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.

Clinical genetics·2004

Twin brothers with MIDAS syndrome and XX karyotype.

American journal of medical genetics. Part A·2003

New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay.

American journal of medical genetics·2001

Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.

American journal of medical genetics·2001

Analysis of Philadelphia chromosome-negative BCR-ABL-positive chronic myelogenous leukemia by hypermetaphase fluorescence in situ hybridization.

Annals of oncology : official journal of the European Society for Medical Oncology·1999

See all related articles