-transparent.png){kind=logo}
A 1-year-old girl with an interstitial deletion of the long arm of chromosome 16 is reported. She was characterized by a distinct craniofacial dysmorphism, meningoencephalocele, mild hydrocephalus, short neck, broad great toes and abnormally positioned toes. High resolution GTG and RBG banding analyses revealed a karyotype: 46,XX,del(16) (q13q22) de novo. An analysis of the smallest region of overlap revealed that the critical band region for 16q deletion syndrome is 16q21.
Related Publications
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
June 1992,
American journal of medical genetics,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
January 1980,
Annales de genetique,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
January 1984,
Human genetics,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
January 1981,
Annales de genetique,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
June 1986,
Clinical genetics,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
January 1994,
Genetic counseling (Geneva, Switzerland),
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
October 1989,
American journal of medical genetics,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
October 2015,
BMC medical genetics,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
May 1999,
British journal of cancer,
K Naritomi, and
N Shiroma, and
Y Izumikawa, and
K Sameshima, and
S Ohdo, and
K Hirayama
May 1987,
Journal of medical genetics,
