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Items: 19

1.

Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita.

Devriendt K, Matthijs G, Legius E, Schollen E, Blockmans D, van Geet C, Degreef H, Cassiman JJ, Fryns JP.

Am J Hum Genet. 1997 Mar;60(3):581-7.

2.

Reticulate hyperpigmentation.

Schnur RE, Heymann WR.

Semin Cutan Med Surg. 1997 Mar;16(1):72-80. Review.

PMID:
9125768
3.

Dyskeratosis congenita is a chromosomal instability disorder.

Dokal I, Luzzatto L.

Leuk Lymphoma. 1994 Sep;15(1-2):1-7. Review.

PMID:
7858487
4.

Dyskeratosis congenita: an inherited bone marrow failure syndrome.

Dokal I.

Br J Haematol. 1996 Mar;92(4):775-9. Review. No abstract available.

PMID:
8616066
5.
6.

[X chromosome inactivation--a biological phenomenon of clinical significance for women].

Orstavik KH.

Tidsskr Nor Laegeforen. 1999 Mar 10;119(7):972-5. Review. Norwegian.

PMID:
10210959
7.

Dyskeratosis congenita: delay in diagnosis and successful treatment of pancytopenia by bone marrow transplantation.

Phillips RJ, Judge M, Webb D, Harper JI.

Br J Dermatol. 1992 Sep;127(3):278-80. Review.

PMID:
1390173
8.

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
9.

Extracutaneous analogies of Blaschko lines.

Rott HD.

Am J Med Genet. 1999 Aug 6;85(4):338-41. Review.

PMID:
10398255
10.

[Dyskeratosis congenita. Genetic hematologic-immunologic systemic disease with pancytopenia].

Sölder B, Weiss M, Jäger A, Belohradsky BH.

Klin Padiatr. 1996 Nov-Dec;208(6):344-9. Review. German.

PMID:
9064376
11.
12.

Dyskeratosis congenita vs. chronic graft versus host disease: report of a case and a review of the literature.

Treister N, Lehmann LE, Cherrick I, Guinan EC, Woo SB.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004 Nov;98(5):566-71. Review.

PMID:
15529128
13.

X-linked dyskeratosis congenita: restrictive pulmonary disease and a novel mutation.

Safa WF, Lestringant GG, Frossard PM.

Thorax. 2001 Nov;56(11):891-4. Review.

14.

X-chromosome inactivation: role in skin disease expression.

Happle R.

Acta Paediatr Suppl. 2006 Apr;95(451):16-23. Review.

PMID:
16720460
15.

Gastrointestinal problems in a child with dyskeratosis congenita.

Berezin S, Schwarz SM, Slim MS, Beneck D, Brudnicki AR, Medow MS.

Am J Gastroenterol. 1996 Jun;91(6):1271-2. Review.

PMID:
8651192
16.

Dyskeratosis congenita.

Drachtman RA, Alter BP.

Dermatol Clin. 1995 Jan;13(1):33-9. Review.

PMID:
7712648
17.

[The X chromosome and X-linked genetic dermatosis].

Prigent F.

Ann Dermatol Venereol. 1983;110(12):1031-5. Review. French. No abstract available.

PMID:
6364927
18.

[The problems of basic genetics seen from the clinical picture of genodermatosis].

García Pérez A.

An R Acad Nac Med (Madr). 1993;110(1):41-57; discussion 58. Review. Spanish. No abstract available.

PMID:
8238821
19.

Polymorphism of the human genome: markers for genetic linkage analyses in heritable diseases of the skin.

Christiano AM, Uitto J.

J Invest Dermatol. 1992 Nov;99(5):519-23. Review. No abstract available.

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