Definition: Whole-arm rearrangements between the acrocentric chromosomes 13-15, 21 and 22, that constitute the most common chromosomal rearrangements in humans.
Context: A carrier of Robertsonian translocation is phenotypically normal, because the translocation chromosome contains nearly all the genetic material of the long arms of two acrocentric chromosomes.
Term: BANDYOPADHYAY, R.B., HELLER, A., KNOX-DUBOIS, C.; MCCASKILL, C., BEREND, S.A., PAGE, S.L. and SHAFFER, L.G. (2002), “Parental Origin and Timing of De Novo Robertsonian Translocation Formation”, The American Society of Human Genetics, 71:6 (p.1456-1462).
Definition: BANDYOPADHYAY, R.B., HELLER, A., KNOX-DUBOIS, C.; MCCASKILL, C., BEREND, S.A., PAGE, S.L. and SHAFFER, L.G. (2002), “Parental Origin and Timing of De Novo Robertsonian Translocation Formation”, The American Society of Human Genetics, 71:6 (p.1456-1462)
Context: KOTHARI, M.L., MEHTA, L. A. & ROUCHOUDHURY, S.S. 2009. “Essentials of Human Genetics”, Orient Longman Private Limited: Hyderabad. Fifth Edition (pp. 273)