Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) <it>de novo </it>in a child with dysmorphic features and streaky pigmentation: case report
<p>Abstract</p> <p>Background</p> <p>Small supernumerary marker chromosomes (sSMC) occur in 0.075% of unselected prenatal and in 0.044% of consecutively studied postnatal cases. Individuals with sSMC present with varying phenotype, ranging from normal to extremely mild...
Main Authors: | Pramathan R, Padariyakam Shabeer, Mani Sara, Al-Rowaished Eman EM, Naveed Sehba, Jacob Preenu S, Malhotra Ashok K, Murthy Sabita K, Nath Ravi, Al-Ali Mahmoud, Al-Gazali Lihadh |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2008-08-01
|
Series: | Molecular Cytogenetics |
Online Access: | http://www.molecularcytogenetics.org/content/1/1/19 |
Similar Items
-
Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy
by: Oliveira Guiomar, et al.
Published: (2009-08-01) -
Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome
by: Chih-Ping Chen, et al.
Published: (2016-10-01) -
aCGH-MAS: Analysis of aCGH by means of Multiagent System
by: Juan F. De Paz, et al.
Published: (2015-01-01) -
The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)
by: Battaglia Agatino
Published: (2008-11-01) -
Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization
by: Chih-Ping Chen, et al.
Published: (2019-09-01)