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K Devriendt

Showing results (211-220 of 230) with videos related to

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Hormone Research in Paediatrics|April 3, 2015
Short Stature in KBG Syndrome: First Responses to Growth Hormone TreatmentNele Reynaert, C W Ockeloen, L Sävendahl, et al.
American Journal of Medical Genetics|July 9, 1999
Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical careG J Van Buggenhout, J C Trommelen, A Schoenmaker, et al.
Journal of Medical Genetics|July 17, 2008
Mapping of 5q35 chromosomal rearrangements within a genomically unstable regionK Buysse, A Crepel, B Menten, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Nature Genetics|March 10, 2001
Constitutively activating mutation in WASP causes X-linked severe congenital neutropeniaK Devriendt, A S Kim, G Mathijs, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)N M C Maas, G Van Buggenhout, F Hannes, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 geneA Orrico, L Galli, L Faivre, et al.
Genetic Counseling (Geneva, Switzerland)|February 22, 2008
The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at randomN M C Maas, S Van Vooren, F Hannes, et al.
Nature|August 10, 2000
GATA3 haplo-insufficiency causes human HDR syndromeH Van Esch, P Groenen, M A Nesbit, et al.
Clinical Genetics|December 8, 2016
Facial dysmorphism is influenced by ethnic background of the patient and of the evaluatorA Lumaka, N Cosemans, A Lulebo Mampasi, et al.
Pageof 23

Showing results (211-220 of 230) with videos related to

Sort By:
Pageof 23
Hormone Research in Paediatrics|April 3, 2015
Short Stature in KBG Syndrome: First Responses to Growth Hormone TreatmentNele Reynaert, C W Ockeloen, L Sävendahl, et al.
American Journal of Medical Genetics|July 9, 1999
Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical careG J Van Buggenhout, J C Trommelen, A Schoenmaker, et al.
Journal of Medical Genetics|July 17, 2008
Mapping of 5q35 chromosomal rearrangements within a genomically unstable regionK Buysse, A Crepel, B Menten, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Nature Genetics|March 10, 2001
Constitutively activating mutation in WASP causes X-linked severe congenital neutropeniaK Devriendt, A S Kim, G Mathijs, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)N M C Maas, G Van Buggenhout, F Hannes, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 geneA Orrico, L Galli, L Faivre, et al.
Genetic Counseling (Geneva, Switzerland)|February 22, 2008
The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at randomN M C Maas, S Van Vooren, F Hannes, et al.
Nature|August 10, 2000
GATA3 haplo-insufficiency causes human HDR syndromeH Van Esch, P Groenen, M A Nesbit, et al.
Clinical Genetics|December 8, 2016
Facial dysmorphism is influenced by ethnic background of the patient and of the evaluatorA Lumaka, N Cosemans, A Lulebo Mampasi, et al.
Pageof 23