Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1989 | 1 |
1997 | 1 |
2010 | 1 |
2024 | 0 |
PubMed (cited) for id: 601952
3 results
Results by year
Filters applied: . Clear all
Page 1
A single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis.
Am J Hum Genet. 2010 Apr 9;86(4):596-603. doi: 10.1016/j.ajhg.2010.02.018. Epub 2010 Mar 11.
Am J Hum Genet. 2010.
PMID: 20226437
Free PMC article.
Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK-syndrome): a rare, autosomal recessive disorder of keratohyaline formation?
Vahlquist A, Pontén F, Pettersson A.
Vahlquist A, et al.
Acta Derm Venereol. 1997 May;77(3):225-7. doi: 10.2340/0001555577225227.
Acta Derm Venereol. 1997.
PMID: 9188877
Free article.
Item in Clipboard
Congenital ichthyosiform dermatosis with linear keratotic flexural papules and sclerosing palmoplantar keratoderma.
Pujol RM, Moreno A, Alomar A, de Moragas JM.
Pujol RM, et al.
Arch Dermatol. 1989 Jan;125(1):103-6.
Arch Dermatol. 1989.
PMID: 2521286
Item in Clipboard
Cite
Cite