Rothmund-Thomson syndrome: a report of two patients and a review of the literature. - Wikidata - awgldk - TriplyDB

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

http://www.wikidata.org/entity/Q37940961

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Rothmund-Thomson syndrome Congenital poikiloderma with unusual hypopigmentation and acral blistering at birth.Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivity.Rothmund-thomson syndrome: a 13-year follow-up Atypical meningioma as a solitary malignancy in a patient with Rothmund-Thompson syndrome Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.Osteogenic sarcoma in the Rothmund-Thomson syndrome.

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Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

http://www.wikidata.org/entity/Q37940961

description

article científic

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article scientifique

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articol științific

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articolo scientifico

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artigo científico

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artigo científico

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artigo científico

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artikel ilmiah

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artículo científico

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name

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

@en

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

@nl

type

label

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

@en

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

@nl

prefLabel

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

@en

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

@nl

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J.1365-2133.1990.TB06272.X

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British Journal of Dermatology

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Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

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Moss C

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P2860

Enhanced radiosensitivity and defective DNA repair in cultured fibroblasts derived from Rothmund Thomson syndrome patients.

Dental anomalies in the Rothmund-Thomson syndrome. Report of a case.

Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome).

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