Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14

Responses

Findings that shed new light on the possible pathogenesis of a disease or an adverse effect

Compose Response

Title *

Author Information

Contributors
First Name and Middle Initial * First or given name, e.g. 'Peter'. Last Name * Your last, or family, name, e.g. 'MacMoody'. Email Address * Your email address, e.g. higgs-boson@gmail.com Occupation * Your role and/or occupation, e.g. 'Orthopedic Surgeon'. Affiliation * Your organization or institution (if applicable), e.g. 'Royal Free Hospital'.

Statement of Competing Interests

Competing interests? *

Yes

Please describe the competing interests

Responses are moderated before posting and publication is at the absolute discretion of BMJ, however they are not peer-reviewed
Once published, you will not have the right to remove or edit your response. Removal or editing of responses is at BMJ's absolute discretion
If patients could recognise themselves, or anyone else could recognise a patient from your description, please obtain the patient's written consent to publication and send them to the editorial office before submitting your response [Patient consent forms]
By submitting this response you are agreeing to our full [Response terms and requirements]

Vertical Tabs

No responses have been published for this article.