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Klaus W Kjaer

Showing results (1-10 of 22) with videos related to

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American Journal of Medical Genetics|December 28, 2002
Limb anomalies: Developmental and evolutionary aspectsFiorella Gurrieri, Klaus W Kjaer, Eugenio Sangiorgi, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1Muhammad Farooq, Shahid Baig, Niels Tommerup, et al.
Acta Odontologica Scandinavica|January 20, 2006
Immunohistochemical expression of p63 in human prenatal tooth primordiaMarianne Kock, Dorrit Nolting, Klaus W Kjaer, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Novel Connexin 43 (GJA1) mutation causes oculo-dento-digital dysplasia with curly hairKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
A novel subtype of distal symphalangism affecting only the 4th fingerKlaus W Kjaer, Mehmet Tiner, Sultan Cingoz, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARGKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Suggestive linkage to a neighboring region of IRF6 in a cleft lip and palate multiplex familyLinda P Jakobsen, Reinhard Ullmann, Klaus W Kjaer, et al.
Human Genetics|January 4, 2008
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expressionHans Eiberg, Jesper Troelsen, Mette Nielsen, et al.
Spine|October 19, 2016
Mutation of the Planar Cell Polarity Gene VANGL1 in Adolescent Idiopathic ScoliosisMalene R Andersen, Muhammad Farooq, Karen Koefoed, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansionsKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|December 28, 2002
Limb anomalies: Developmental and evolutionary aspectsFiorella Gurrieri, Klaus W Kjaer, Eugenio Sangiorgi, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1Muhammad Farooq, Shahid Baig, Niels Tommerup, et al.
Acta Odontologica Scandinavica|January 20, 2006
Immunohistochemical expression of p63 in human prenatal tooth primordiaMarianne Kock, Dorrit Nolting, Klaus W Kjaer, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Novel Connexin 43 (GJA1) mutation causes oculo-dento-digital dysplasia with curly hairKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
A novel subtype of distal symphalangism affecting only the 4th fingerKlaus W Kjaer, Mehmet Tiner, Sultan Cingoz, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARGKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Suggestive linkage to a neighboring region of IRF6 in a cleft lip and palate multiplex familyLinda P Jakobsen, Reinhard Ullmann, Klaus W Kjaer, et al.
Human Genetics|January 4, 2008
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expressionHans Eiberg, Jesper Troelsen, Mette Nielsen, et al.
Spine|October 19, 2016
Mutation of the Planar Cell Polarity Gene VANGL1 in Adolescent Idiopathic ScoliosisMalene R Andersen, Muhammad Farooq, Karen Koefoed, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansionsKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
Pageof 3