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The syndrome of congenital telangiectaticerythema and stunted growth

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The syndrome of congenital telangiectatic erythema and stunted growth (English)

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The syndrome of congenital telangiectaticerythema and stunted growth (English)

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DOI

10.1016/S0022-3476(66)80426-2

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https://api.crossref.org/works/10.1016/S0022-3476(66)80426-2

11 July 2023

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Europe PubMed Central

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5901336

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901336

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11 July 2023

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D. Bloom

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1

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Europe PubMed Central

PubMed ID

5901336

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901336

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English

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January 1966

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https://api.elsevier.com/content/article/PII:S0022347666804262?httpAccept=text/xml

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10.1016/S0022-3476(66)80426-2

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11 July 2023

https://api.elsevier.com/content/article/PII:S0022347666804262?httpAccept=text/plain

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10.1016/S0022-3476(66)80426-2

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The Journal of Pediatrics

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volume

68

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page(s)

103-13

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1

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cites work

A contribution to Bloom's syndrome. Congenital telangiectatic erythema resembling lypus erythematosus in dwarfs

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7 January 2021

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Dwarfism with skin manifestations

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CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS.

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CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN

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POIKILODERMA CONGENITALE. REPORT OF TWO CASES

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Werner's syndrome; report of two cases

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7 January 2021

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Inheritance of an Abnormal Chromosome in Down's Syndrome (Mongolism) with Leukemia

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11

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10.1016/S0022-3476(66)80426-2

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11 July 2023

Non-endocrine dwarfism and pseudoepiphyses

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23

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10.1016/S0022-3476(66)80426-2

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11 July 2023

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DOI

10.1016/S0022-3476(66)80426-2

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PubMed ID

5901336

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(Q57462560)

The syndrome of congenital telangiectaticerythema and stunted growth

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