-transparent.png){kind=logo}
Trisomy 18q2 in a boy associated with a reciprocal translocation due to a paternal balanced complex rearrangement interesting chromosome 9, 10 and 18 is reported. Using this observation phenotypical data of the "typical" clinical description are discussed and some particular signs are pointed out. About the occurrence of the complex chromosomal rearrangement different hypothesis are considered.
Related Publications
G Bourrouillou, and
M Rolland, and
P Colombies
January 1983,
Annales de genetique,
G Bourrouillou, and
M Rolland, and
P Colombies
October 1976,
Human genetics,
G Bourrouillou, and
M Rolland, and
P Colombies
May 1991,
Annales de pediatrie,
G Bourrouillou, and
M Rolland, and
P Colombies
March 1993,
Boletin medico del Hospital Infantil de Mexico,
G Bourrouillou, and
M Rolland, and
P Colombies
December 1975,
Humangenetik,
G Bourrouillou, and
M Rolland, and
P Colombies
January 1978,
American journal of medical genetics,
G Bourrouillou, and
M Rolland, and
P Colombies
March 1988,
Jinrui idengaku zasshi. The Japanese journal of human genetics,
G Bourrouillou, and
M Rolland, and
P Colombies
December 1991,
American journal of medical genetics,
G Bourrouillou, and
M Rolland, and
P Colombies
August 2019,
BMJ case reports,
G Bourrouillou, and
M Rolland, and
P Colombies
April 2001,
Journal of paediatrics and child health,
