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Burkitt t(8;14)(q24;q32) and cryptic deletion in a CLL patient: report of a case and review of literature

โœ Scribed by Kavita Reddy; Radha Satyadev; Derek Bouman; Michele K. Hibbard; Gary Lu; Romero Paolo


Book ID
113512822
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
390 KB
Volume
166
Category
Article
ISSN
0165-4608

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Proximal interstitial deletion of 7q: A
โœ Zackowski, Joleen L. ;Raffel, Leslie J. ;Blank, Carol A. ;Schwartz, Stuart ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 447 KB ๐Ÿ‘ 2 views

A male infant with multiple congenital anomalies was found to have a deletion of 7q [46,XY,del(7)(pter+ql1.2:: q22-3qter)l. The father had a balanced rearrangement involving chromosomes 7 and 9, interpreted as 46,XY,dir ins(9;7) (9pter+ 9p12::7q22+ 7q11.2:: 9p12-3 9qteq7pter-3 7q11.2 :: 7q22-3 7qter