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P Korge

Showing results (31-40 of 35) with videos related to

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The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.
Human Molecular Genetics|June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated familiesE Maestrini, B P Korge, J Ocaña-Sierra, et al.
The Journal of Investigative Dermatology|November 6, 1998
A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patientsB P Korge, E Healy, C S Munro, et al.
Nature Genetics|July 1, 1992
Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12qJ G Compton, J J DiGiovanna, S K Santucci, et al.
The Journal of Investigative Dermatology|October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotypeB P Korge, H Hamm, C S Jury, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
The Journal of Investigative Dermatology|October 27, 1997
Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosisB P Korge, A Ishida-Yamamoto, C Pünter, et al.
Human Molecular Genetics|June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated familiesE Maestrini, B P Korge, J Ocaña-Sierra, et al.
The Journal of Investigative Dermatology|November 6, 1998
A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patientsB P Korge, E Healy, C S Munro, et al.
Nature Genetics|July 1, 1992
Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12qJ G Compton, J J DiGiovanna, S K Santucci, et al.
The Journal of Investigative Dermatology|October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotypeB P Korge, H Hamm, C S Jury, et al.
Pageof 4