Familial 10p trisomy resulting from a maternal pericentric inversion

This publication has 22 references indexed in Scilit:

• Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10
  Clinical Genetics, 2008
• Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12)
  American Journal of Medical Genetics, 1983
• Duplication deficiency as the result of meiotic segregation of a maternal InV (10)
  Human Genetics, 1981
• Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12)
  Human Genetics, 1979
• Partial duplication of the short arm of chromosome 10
  Human Genetics, 1979
• Trisomy 10p due to a de novo t(10p;13p)
  Human Genetics, 1979
• Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship
  Human Genetics, 1978
• Brother and sister with trisomy 10p
  Human Genetics, 1978
• Partial trisomy 10p
  Human Genetics, 1975
• Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10),rec(10), in her son
  Cytogenetic and Genome Research, 1973