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K Devriendt

Showing results (151-160 of 230) with videos related to

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Genomics|December 1, 1996
Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, P Debeer, et al.
Annales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.
Clinical Genetics|December 17, 2009
DISC1 duplication in two brothers with autism and mild mental retardationA Crepel, J Breckpot, J-P Fryns, et al.
American Journal of Medical Genetics|May 22, 1995
Diaphragmatic hernia in Denys-Drash syndromeK Devriendt, E Deloof, P Moerman, et al.
Prenatal Diagnosis|January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)Ingrid Witters, K Devriendt, E Legius, et al.
Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.
Journal of Medical Genetics|June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophyG Matthijs, E Schollen, E Legius, et al.
Retina (Philadelphia, Pa.)|April 28, 2000
Familial spastic paraplegia and maculopathy with juxtafoveolar retinal telangiectasis and subretinal neovascularizationA Leys, H D Gilbert, W Van De Sompel, et al.
Cytogenetic and Genome Research|September 17, 2011
Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defectsJ Breckpot, B Thienpont, Y Arens, et al.
American Journal of Medical Genetics|February 22, 2002
Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler typeI Witters, Ph Moerman, K Devriendt, et al.
Pageof 23

Showing results (151-160 of 230) with videos related to

Sort By:
Pageof 23
Genomics|December 1, 1996
Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, P Debeer, et al.
Annales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.
Clinical Genetics|December 17, 2009
DISC1 duplication in two brothers with autism and mild mental retardationA Crepel, J Breckpot, J-P Fryns, et al.
American Journal of Medical Genetics|May 22, 1995
Diaphragmatic hernia in Denys-Drash syndromeK Devriendt, E Deloof, P Moerman, et al.
Prenatal Diagnosis|January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)Ingrid Witters, K Devriendt, E Legius, et al.
Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.
Journal of Medical Genetics|June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophyG Matthijs, E Schollen, E Legius, et al.
Retina (Philadelphia, Pa.)|April 28, 2000
Familial spastic paraplegia and maculopathy with juxtafoveolar retinal telangiectasis and subretinal neovascularizationA Leys, H D Gilbert, W Van De Sompel, et al.
Cytogenetic and Genome Research|September 17, 2011
Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defectsJ Breckpot, B Thienpont, Y Arens, et al.
American Journal of Medical Genetics|February 22, 2002
Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler typeI Witters, Ph Moerman, K Devriendt, et al.
Pageof 23