Buscar
Mostrando ítems 1-10 de 25
The pattern of callosal connections in posterior neocortex of congenitally anophthalmic rats 1897 as a valid species of the genus Callitetrarhynchus
(1988)
In an effort to assess the innate capacity of the central visual system to specify corticocortical connectivity in the absence of retinal afferents, we examined the tangential distribution of callosal cells and terminations ...
CT findings of the main pathological conditions associated with horseshoe kidneys
(British Institute of Radiology, 2015)
Horseshoe kidney (HSK) is the most common renal fusion anomaly, with a prevalence of 0.25% among the general population. It consists of kidney fusion across the midline. HSK can be present as an isolated condition in 30%, ...
CT findings of the main pathological conditions associated with horseshoe kidneys
(British Institute of Radiology, 2015)
Horseshoe kidney (HSK) is the most common renal fusion anomaly, with a prevalence of 0.25% among the general population. It consists of kidney fusion across the midline. HSK can be present as an isolated condition in 30%, ...
Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome
(Elsevier, 2012)
OBJECTIVE:
Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable cause of cleft palate. ...
Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome
(Elsevier, 2012)
OBJECTIVE:
Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable cause of cleft palate. ...
The genetic basis of DOORS syndrome: an exome-sequencing study
(Elsevier, 2017)
Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients
(Nature, 2017)
22q11.2 microdeletion syndrome (22q11.2DS) is the most common microdeletion disorder in humans, with an incidence of 1/4000 live births. It is caused by a heterozygous deletion of 1.5–3 Mb on chromosome region 22q11.2. ...