Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies.

Jaiswal, Sushil Kumar; Kumar, Ashok; Ali, Akhtar; Rai, Amit Kumar

Jaiswal, Sushil Kumar; Kumar, Ashok; Ali, Akhtar; Rai, Amit Kumar.

Affiliation

Jaiswal SK; Centre for Genetic Disorders, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: sushil.biotech@yahoo.co.in.
Kumar A; Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: ashokkumar_bhu@hotmail.com.
Ali A; Centre for Genetic Disorders, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: akhtar@bhu.ac.in.
Rai AK; Centre for Genetic Disorders, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India. Electronic address: akrai10@gmail.com.

Gene ; 559(1): 94-8, 2015 Mar 15.

Article de En | MEDLINE | ID: mdl-25617521

Sujet(s)
Mots clés

Cytogenetic microarray; Marker chromosome; Mosaicism

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Malformations multiples / Chromosomes humains de la paire 2 / Chromosomes humains de la paire 18 / Noyau de la cellule / Délétion de segment de chromosome Type d'étude: Prognostic_studies Limites: Humans / Infant / Male Langue: En Journal: Gene Année: 2015 Type de document: Article

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