Format
Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 13

1.

Dyskeratosis congenita: a genetic disorder of many faces.

Kirwan M, Dokal I.

Clin Genet. 2008 Feb;73(2):103-12. Epub 2007 Nov 14. Review.

PMID:
18005359
2.

Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10.

Walne AJ, Vulliamy T, Marrone A, Beswick R, Kirwan M, Masunari Y, Al-Qurashi FH, Aljurf M, Dokal I.

Hum Mol Genet. 2007 Jul 1;16(13):1619-29. Epub 2007 May 16.

3.

THE ASSOCIATION OF DYSKERATOSIS CONGENITA AND FANCONI'S ANAEMIA.

ADDISON M, RICE MS.

Med J Aust. 1965 May 29;1(22):797-9. No abstract available.

PMID:
14312691
4.

DYSKERATOSIS CONGENITA. FIRST REPORT OF ITS OCCURRENCE IN A FEMALE AND A REVIEW OF THE LITERATURE.

SORROW JM Jr, HITCH JM.

Arch Dermatol. 1963 Sep;88:340-7. No abstract available.

PMID:
14043629
5.

Dyskeratosis congenita.

COSTELLO MJ, BUNCKE CM.

AMA Arch Derm. 1956 Feb;73(2):123-32. No abstract available.

PMID:
13282498
6.

Human H/ACA small nucleolar RNPs and telomerase share evolutionarily conserved proteins NHP2 and NOP10.

Pogacić V, Dragon F, Filipowicz W.

Mol Cell Biol. 2000 Dec;20(23):9028-40.

7.

Dyskeratosis congenita: an autosomal recessive variant.

Elliott AM, Graham GE, Bernstein M, Mazer B, Teebi AS.

Am J Med Genet. 1999 Mar 19;83(3):178-82.

PMID:
10096592
8.

Nhp2p and Nop10p are essential for the function of H/ACA snoRNPs.

Henras A, Henry Y, Bousquet-Antonelli C, Noaillac-Depeyre J, Gélugne JP, Caizergues-Ferrer M.

EMBO J. 1998 Dec 1;17(23):7078-90.

9.

Function and synthesis of small nucleolar RNAs.

Tollervey D, Kiss T.

Curr Opin Cell Biol. 1997 Jun;9(3):337-42. Review.

PMID:
9159079
10.
11.

Etiologic heterogeneity in dyskeratosis congenita.

Pai GS, Morgan S, Whetsell C.

Am J Med Genet. 1989 Jan;32(1):63-6.

PMID:
2705484
12.

Dyskeratosis congenita: clinical and genetic heterogeneity. Report of a new case and review of the literature.

Drachtman RA, Alter BP.

Am J Pediatr Hematol Oncol. 1992 Nov;14(4):297-304. Review.

PMID:
1456394
13.

Active and suppressor T cells: diminution in a patient with dyskeratosis congenita and in first-degree relatives.

Fudenberg HH, Goust JM, Vesole DH, Salinas CF.

Gerontology. 1979;25(4):231-7.

PMID:
313356

Supplemental Content

Support Center