(Q28213315)

https://api.crossref.org/works/10.1002%2FAJMG.10065

Baller-Gerold syndrome: an 11th case of craniosynostosis and radial aplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Is there a Baller-Gerold syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Baller-Gerold syndrome: case report and clinical and radiological review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Mid-portion agenesis of corpus callosum in a presumed Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Magnetic resonance imaging to visualize the internal anatomy in the Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Contributing software to the internet: the Amplify program

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Craniosynostosis-radial aplasia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Mutations in the human TWIST gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Baller-Gerold syndrome associated with congenital hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Further delineation of the Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Baller-Gerold syndrome associated with congenital portal venous malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

The classification of amino acid conservation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

The Baller-Gerold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Cloning of the human twist gene: its expression is retained in adult mesodermally-derived tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065

Craniosynostosis with associated cranial base anomalies: a morphologic and histologic study of affected like-sexed twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10065