Molecular genetic analysis in autosomal dominant keratoconus.

Molecular analysis of autosomal dominant neurohypophyseal diabetes insipidus.

Genetic diagnosis of autosomal dominant polycystic kidney disease: linkage analysis versus direct mutation analysis.

Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France.

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study.

Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity.

Autosomal dominant microcephaly.

Autosomal dominant osteosclerosis.

Autosomal dominant ichthyosis exfoliativa.

Autosomal dominant acrodysostosis.

Mutation analysis in Chinese families with autosomal dominant hereditary cataracts.

Autosomal dominant neurological disorders.

Autosomal dominant congenital laryngomalacia.

Autosomal Dominant Osteopetrosis Type II.

Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing.

Autosomal dominant neovascular inflammatory vitreoretinopathy.

Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells.

[Autosomal-dominant polycystic kidney disease].

Electro-oculography in autosomal dominant vitreoretinochoroidopathy.

Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype--the importance of dystrophin and molecular genetic analysis.

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

[Autosomal dominant polycystic kidney disease in infancy].

Genetic mechanisms and signaling pathways in autosomal dominant polycystic kidney disease.

Genetic and clinical studies in autosomal dominant polycystic kidney disease type 1 (ADPKD1).

Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening.

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Molecular analysis of autosomal dominant neurohypophyseal diabetes insipidus.

Genetic diagnosis of autosomal dominant polycystic kidney disease: linkage analysis versus direct mutation analysis.

Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France.

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study.

Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity.

Autosomal dominant microcephaly.

Autosomal dominant osteosclerosis.

Autosomal dominant ichthyosis exfoliativa.

Autosomal dominant acrodysostosis.

Mutation analysis in Chinese families with autosomal dominant hereditary cataracts.

Autosomal dominant neurological disorders.

Autosomal dominant congenital laryngomalacia.

Autosomal Dominant Osteopetrosis Type II.

Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing.

Autosomal dominant neovascular inflammatory vitreoretinopathy.

Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells.

[Autosomal-dominant polycystic kidney disease].

Electro-oculography in autosomal dominant vitreoretinochoroidopathy.

Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype--the importance of dystrophin and molecular genetic analysis.

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

[Autosomal dominant polycystic kidney disease in infancy].

Genetic mechanisms and signaling pathways in autosomal dominant polycystic kidney disease.

Genetic and clinical studies in autosomal dominant polycystic kidney disease type 1 (ADPKD1).

Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening.

Molecular genetic analysis in autosomal dominant keratoconus.

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