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Last Updated: 10/31/2025

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Found 9 publications

Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations.

Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations.

Journal: American journal of medical genetics. Part A
Published: July 13, 2006

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

Journal: American journal of medical genetics
Published: October 26, 2000

On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.

On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.

Journal: Genetic counseling (Geneva, Switzerland)
Published: January 01, 1997

Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus.

Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus.

Journal: American journal of human genetics
Published: November 01, 1995

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.

Journal: Cell
Published: February 10, 1995

The "Fantasy Island" syndrome. Identification of a new osteochondrodysplasia probably of autosomal dominant type

The "Fantasy Island" syndrome. Identification of a new osteochondrodysplasia probably of autosomal dominant type

Journal: Gaceta medica de Mexico
Published: January 01, 1995

Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.

Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.

Journal: American journal of medical genetics
Published: July 01, 1990

Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndrome.

Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndrome.

Journal: Journal of medical genetics
Published: August 01, 1986

Dentine dysplasia with sclerotic bone and skeletal anomalies inherited as an autosomal dominant trait. A new syndrome.

Dentine dysplasia with sclerotic bone and skeletal anomalies inherited as an autosomal dominant trait. A new syndrome.

Journal: Oral surgery, oral medicine, and oral pathology
Published: February 01, 1977
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Last Updated: 10/31/2025