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J Kohlhase

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Cytogenetics and Cell Genetics|May 27, 1999
Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2J Kohlhase, A Köhler, H Jäckle, et al.
American Journal of Medical Genetics|April 11, 2000
First confirmed case with paternal uniparental disomy of chromosome 16J Kohlhase, B Janssen, K Weidenauer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
Genomic cloning, chromosomal mapping, and expression analysis of msal-2J Kohlhase, M Altmann, L Archangelo, et al.
Nature Genetics|January 13, 1998
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndromeJ Kohlhase, A Wischermann, H Reichenbach, et al.
The British Journal of Dermatology|October 20, 2018
Alitretinoin in punctate palmoplantar keratodermaP Yilmaz, M Medvecz, J Kohlhase, et al.
Cytogenetic and Genome Research|June 27, 2003
Cloning and expression analysis of SALL4, the murine homologue of the gene mutated in Okihiro syndromeJ Kohlhase, M Heinrich, M Liebers, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Multiple malignant diseases in a patient with Rothmund-Thomson syndrome with RECQL4 mutations: Case report and literature reviewT Simon, J Kohlhase, C Wilhelm, et al.
Dermatology (Basel, Switzerland)|October 13, 2010
Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancerC Has, B Burger, A Volz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 21, 2015
Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgarisS Goetze, F Raessler, U C Hipler, et al.
HNO|July 23, 2013
[Middle ear salivary gland choristoma related to branchio-oto-renal syndrome diagnosed by array-CGH]P Amrhein, C Sittel, C Spaich, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Cytogenetics and Cell Genetics|May 27, 1999
Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2J Kohlhase, A Köhler, H Jäckle, et al.
American Journal of Medical Genetics|April 11, 2000
First confirmed case with paternal uniparental disomy of chromosome 16J Kohlhase, B Janssen, K Weidenauer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
Genomic cloning, chromosomal mapping, and expression analysis of msal-2J Kohlhase, M Altmann, L Archangelo, et al.
Nature Genetics|January 13, 1998
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndromeJ Kohlhase, A Wischermann, H Reichenbach, et al.
The British Journal of Dermatology|October 20, 2018
Alitretinoin in punctate palmoplantar keratodermaP Yilmaz, M Medvecz, J Kohlhase, et al.
Cytogenetic and Genome Research|June 27, 2003
Cloning and expression analysis of SALL4, the murine homologue of the gene mutated in Okihiro syndromeJ Kohlhase, M Heinrich, M Liebers, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Multiple malignant diseases in a patient with Rothmund-Thomson syndrome with RECQL4 mutations: Case report and literature reviewT Simon, J Kohlhase, C Wilhelm, et al.
Dermatology (Basel, Switzerland)|October 13, 2010
Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancerC Has, B Burger, A Volz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 21, 2015
Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgarisS Goetze, F Raessler, U C Hipler, et al.
HNO|July 23, 2013
[Middle ear salivary gland choristoma related to branchio-oto-renal syndrome diagnosed by array-CGH]P Amrhein, C Sittel, C Spaich, et al.
Pageof 5