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International Journal of Pediatric Otorhinolaryngology
|
July 10, 2013
Aetiology of congenital hearing loss: a cohort review of 569 subjects
F Lammens, N Verhaert, K Devriendt, et al.
Journal of Medical Genetics
|
March 25, 2005
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions
S Girirajan, L J Elsas, K Devriendt, et al.
American Journal of Medical Genetics
|
March 8, 2000
Neuroblastoma in a mother and congenital central hypoventilation in her daughter: variable expression of the same genetic disorder?
K Devriendt, J P Fryns, G Naulaers, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Polyhydramnios and paroxysmal atrial tachycardia as first clinical signs in Costello syndrome
J P Fryns, H Devlieger, M Gewillig, et al.
Cytogenetic and Genome Research
|
November 3, 2010
A balanced translocation t(6;14)(q25.3;q13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum
L Backx, E Seuntjens, K Devriendt, et al.
FEBS Letters
|
March 26, 1990
A genetic polymorphism in a functional domain of human pregnancy zone protein: the bait region. Genomic structure of the bait domains of human pregnancy zone protein and alpha 2 macroglobulin
P Marynen, K Devriendt, H Van den Berghe, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
February 27, 2007
Prenatal diagnosis of schizencephaly after inhalation of organic solvents
I Witters, M Cannie, P Casaer, et al.
Cytogenetic and Genome Research
|
September 7, 2006
Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies
B Thienpont, M Gewillig, J-P Fryns, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 1, 2007
A case of left isomerism with early fetal decompensation
I Witters, P Debois, J P Fryns, et al.
Journal of Medical Genetics
|
April 1, 1996
Renal and urological tract malformations caused by a 22q11 deletion
K Devriendt, A Swillen, J P Fryns, et al.
Page
of 23
Search research articles
Search
Showing results (51-60 of 230) with videos related to
Sort By:
Page
of 23
International Journal of Pediatric Otorhinolaryngology
|
July 10, 2013
Aetiology of congenital hearing loss: a cohort review of 569 subjects
F Lammens, N Verhaert, K Devriendt, et al.
Journal of Medical Genetics
|
March 25, 2005
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions
S Girirajan, L J Elsas, K Devriendt, et al.
American Journal of Medical Genetics
|
March 8, 2000
Neuroblastoma in a mother and congenital central hypoventilation in her daughter: variable expression of the same genetic disorder?
K Devriendt, J P Fryns, G Naulaers, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Polyhydramnios and paroxysmal atrial tachycardia as first clinical signs in Costello syndrome
J P Fryns, H Devlieger, M Gewillig, et al.
Cytogenetic and Genome Research
|
November 3, 2010
A balanced translocation t(6;14)(q25.3;q13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum
L Backx, E Seuntjens, K Devriendt, et al.
FEBS Letters
|
March 26, 1990
A genetic polymorphism in a functional domain of human pregnancy zone protein: the bait region. Genomic structure of the bait domains of human pregnancy zone protein and alpha 2 macroglobulin
P Marynen, K Devriendt, H Van den Berghe, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
February 27, 2007
Prenatal diagnosis of schizencephaly after inhalation of organic solvents
I Witters, M Cannie, P Casaer, et al.
Cytogenetic and Genome Research
|
September 7, 2006
Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies
B Thienpont, M Gewillig, J-P Fryns, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 1, 2007
A case of left isomerism with early fetal decompensation
I Witters, P Debois, J P Fryns, et al.
Journal of Medical Genetics
|
April 1, 1996
Renal and urological tract malformations caused by a 22q11 deletion
K Devriendt, A Swillen, J P Fryns, et al.
Page
of 23