-transparent.png){kind=logo}
A girl, who died at 25 days of age, was found to have a partial monosomy due to a 11q23 leads to 11qter deletion. The main clinical findings were trigonocephay, facial dysmorphia, and congenital heart disease. A review of developmental and dysmorphic features of the seventeen recognized cases is presented.
Related Publications
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
December 1977,
Clinical genetics,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
November 1982,
American journal of medical genetics,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
January 1980,
Human genetics,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
December 1977,
Journal of medical genetics,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
October 1978,
Anales espanoles de pediatria,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
November 1993,
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
January 1990,
American journal of medical genetics,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
January 1976,
American journal of mental deficiency,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
April 1984,
Clinical genetics,
C Léonard, and
C Courpotin, and
B Labrune, and
G Lepercq, and
J Kachaner, and
P Caut
January 1982,
Annales de genetique,
