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Publication

Craniofacial abnormalities in a murine model of Saethre-Chotzen Syndrome.

Sarah Lonsdale | Robin Yong | Alexander Khominsky | Suzanna Mihailidis | Grant Townsend | Sarbin Ranjitkar | Peter J Anderson
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft | 2019

Saethre-Chotzen Syndrome (SCS) is an autosomal dominant syndrome that occurs due to a mutation or deletion of the Twist1 gene at chromosome 7p21. Our aim was to conduct a morphometric analysis of the craniofacial features in the mouse associated with a Twist1+/- mutation.

Pubmed ID: 31199981

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Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.

Swiss nude (tool)

RRID:MGI:5649767

laboratory mouse with name Swiss nude from MGI.

View all literature mentions

C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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The Stimulating Peripheral Activity to Relieve Conditions (SPARC) effort is the result of National Institutes of Health’s (NIH) drive to map out the neural circuitry responsible for visceral control in higher vertebrates. The SPARC Anatomy Working Group (SAWG) is responsible for the integrity of anatomical knowledge in SPARC

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