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Literature DB >> 13300470

[Recessive, sex-limited microphthalmia with multiple abnormalities].

W LENZ.

Abstract

Entities: Disease

Keywords: ABNORMALITIES; EYE/abnormalities

Mesh：

Year: 1955 PMID： 13300470

Source DB: PubMed Journal: Z Kinderheilkd ISSN： 0044-2917

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Cited

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14 in total

1. A case of Lenz microphthalmia syndrome.

Authors: F F Ozkinay; C Ozkinay; H Yüksel; A Yenigun; G Sapmaz; O Aksu
Journal: J Med Genet Date: 1997-07 Impact factor: 6.318

2. Avoiding pitfalls in molecular genetic testing: case studies of high-resolution array comparative genomic hybridization testing in the definitive diagnosis of Mowat-Wilson syndrome.

Authors: Michael Joseph Kluk; Yu An; Philip James; David Coulter; David Harris; Bai-Lin Wu; Yiping Shen
Journal: J Mol Diagn Date: 2011-05 Impact factor: 5.568

3. Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11.

Authors: M I Othman; S A Sullivan; G L Skuta; D A Cockrell; H M Stringham; C A Downs; A Fornés; A Mick; M Boehnke; D Vollrath; J E Richards
Journal: Am J Hum Genet Date: 1998-11 Impact factor: 11.025

4. Lenz microphthalmia syndrome?

Authors: Ramachandran Sudarshan; Rajeshwari G Annigeri
Journal: Wien Klin Wochenschr Date: 2011-02 Impact factor: 1.704

5. Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors: R A Lewis
Journal: Trans Am Ophthalmol Soc Date: 1989

Review 10. Genetics of microphthalmos.

Authors: M Warburg
Journal: Int Ophthalmol Date: 1981-08 Impact factor: 2.031

[Recessive, sex-limited microphthalmia with multiple abnormalities].

1. A case of Lenz microphthalmia syndrome.

2. Avoiding pitfalls in molecular genetic testing: case studies of high-resolution array comparative genomic hybridization testing in the definitive diagnosis of Mowat-Wilson syndrome.

3. Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11.

4. Lenz microphthalmia syndrome?

5. Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

6. Genetical aspects of severe visual impairment in childhood.

Review 7. Recent advances in ophthalmic genetics. Genetic counselling.

8. X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

9. Megarbane syndrome.

Review 10. Genetics of microphthalmos.