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Output details

1 - Clinical Medicine

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Article title

Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism.

Type

D - Journal article

DOI

Title of journal

J Clin Endocrinol Metab

Article number

Volume number

Issue number

First page of article

4031

ISSN of journal

1945-7197

Year of publication

2010

URL

Number of additional authors

Additional information

Justification Statement

(a) The author made a substantial contribution to

(i) the conception and design of the study

(ii) the organisation and conduct of the study

(iii) carrying out the study (including acquisition of study data)

(iv) analysis and interpretation of study data

and

(b) The author helped

(i) draft the output

(ii) critique the output for important intellectual content

Interdisciplinary

Cross-referral requested

Research group

None

Citation count

Proposed double-weighted

Double-weighted statement

Reserve for a double-weighted output

Non-English

English abstract