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K Devriendt

Showing results (201-210 of 230) with videos related to

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Facts, Views & Vision in Obgyn|April 23, 2014
The fetal respiratory system as target for antenatal therapyJ Toelen, M Carlon, F Claus, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsPhilippe Debeer, H Peeters, S Driess, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23)B Dimitrov, K Devriendt, N M C Maas, et al.
American Journal of Medical Genetics|September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Personality profiles of youngsters with velo-cardio-facial syndromeP Prinzie, A Swillen, A Vogels, et al.
Prenatal Diagnosis|March 21, 2025
Persistent Uninterpretable or Failed Prenatal Cell-Free DNA Screening Indicates a High-Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA-Analysis: A Prospective Cohort StudyL Lannoo, K Van Den Bogaert, A Belmans, et al.
Journal of Medical Genetics|September 3, 2004
Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype mapG Van Buggenhout, C Melotte, B Dutta, et al.
Human Genetics|February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.
Clinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.
American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.
Pageof 23

Showing results (201-210 of 230) with videos related to

Sort By:
Pageof 23
Facts, Views & Vision in Obgyn|April 23, 2014
The fetal respiratory system as target for antenatal therapyJ Toelen, M Carlon, F Claus, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsPhilippe Debeer, H Peeters, S Driess, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23)B Dimitrov, K Devriendt, N M C Maas, et al.
American Journal of Medical Genetics|September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Personality profiles of youngsters with velo-cardio-facial syndromeP Prinzie, A Swillen, A Vogels, et al.
Prenatal Diagnosis|March 21, 2025
Persistent Uninterpretable or Failed Prenatal Cell-Free DNA Screening Indicates a High-Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA-Analysis: A Prospective Cohort StudyL Lannoo, K Van Den Bogaert, A Belmans, et al.
Journal of Medical Genetics|September 3, 2004
Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype mapG Van Buggenhout, C Melotte, B Dutta, et al.
Human Genetics|February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.
Clinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.
American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.
Pageof 23