(Q28139531)

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Cardiac valvular disease and Axenfeld-Rieger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

The Axenfeld syndrome and the Rieger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

MESODERMAL DYSGENESIS OF THE ANTERIOR SEGMENT: RIEGER'S ANOMALY

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Rieger's syndrome. A case report with a 15-year follow-up

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Anterior chamber cleavage syndrome. A stepladder classification.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-tel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Autosomal dominant iridogoniodysgenesis with associated somatic anomalies: four-generation family with Rieger's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Histopathology and molecular basis of iridogoniodysgenesis syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Familial glaucoma. In nine generations of a South Hampshire family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

The human PAX6 gene is mutated in two patients with aniridia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma

7 January 2021

2 references

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

inferred from DOI database lookup

7 January 2021

based on heuristic

Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Origins of avian ocular and periocular tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

The anterior chamber cleavage syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Neural crest origin of trabecular meshwork cells and other structures of the anterior chamber

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0

Herwigh Rieger, 2 May 1898-1 February 1986.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900525-0