Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints

Author:

Amos-Landgraf James M.,Ji Yonggang,Gottlieb Wayne,Depinet Theresa,Wandstrat Amy E.,Cassidy Suzanne B.,Driscoll Daniel J.,Rogan Peter K.,Schwartz Stuart,Nicholls Robert D.

Funder

March of Dimes Foundation

National Institutes of Health

Publisher

Elsevier BV

Reference72 articles.

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3. High level of unequal meiotic crossovers at the origin of the 22q11.2 and 7q11.23 deletions;Baumer;Hum Mol Genet,1998

4. Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease 1A: first report of a de novo duplication with a maternal origin;Blair;Am J Hum Genet,1996

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