Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous

Investigative Ophthalmology and Visual Science

Volumn 42, Issue 10, 2001, Pages 2225-2228

  Khaliq, S ^a   Hameed, A ^a   Ismail, M ^a   Anwar, K ^a   Leroy, B ^a   Payne, A M ^a   Bhattacharya, S S ^a   Mehdi, S Q ^a  

^a Dr A Q Khan Research Laboratories   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADHESION; ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CATARACT; CHILD; CHROMOSOME 10Q; CLINICAL ARTICLE; CORNEA OPACITY; FEMALE; GENE LOCUS; GENETIC LINKAGE; GENETIC RECOMBINATION; HOMOZYGOSITY; HUMAN; MALE; PERSISTENT HYPERPLASTIC PRIMARY VITREOUS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ANTERIOR EYE SEGMENT; CATARACT; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; CONSANGUINITY; CORNEAL OPACITY; DNA; EYE ABNORMALITIES; FEMALE; GENES, RECESSIVE; HUMANS; HYPERPLASIA; LINKAGE (GENETICS); LOD SCORE; MALE; MICROPHTHALMOS; MICROSATELLITE REPEATS; PEDIGREE; POLYMERASE CHAIN REACTION; VITREOUS BODY;

EID: 0034854917     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. Persistent hyperplastic primary vitreous (PHPV)
2. Persistent fetal vasculature (PFV): An integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture
3. Childhood blindness and visual loss: An assessment at two institutions including a "new" cause
4. Neurologic abnormalities associated with persistent hyperplastic primary vitreous
5. Diagnostic criteria for Walker-Warburg syndrome
6. Multiple congenital anomaly syndrome caused by an extra autosome
7. Study of the Norrie disease gene in 2 patients with bilateral persistent hyperplastic primary vitreous
8. Persistent hyperplastic primary vitreous with retinal tumor in tuberous sclerosis: Report of a case including tumoral immunohistochemistry and cytogenetic analyses
9. Persistent hyperplastic primary vitreous in a family with osteoporosis-pseudoglioma syndrome
10. Familial persistent pupillary membranes
11. Persistent hyperplastic primary vitreous with vertical transmission
12. Primary vitreoretinal dysplasia transmitted as an autosomal recessive disorder
13. Persistent hyperplastic primary vitreous in non-identical twins
14. A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32
15. Intelligent linkage analysis using gene density estimates
16. Easy calculation of LOD scores and genetic risks on small computers
17. Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21
18. Localization of the human RGR opsin gene to chromosome 10q23
19. Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa
20. Usher syndrome ID and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel Cadherin-like gene CDH23
21. Localization of the Usher syndrome type 1D gene (USH1D) to chromosome 10
22. Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene
23. Localization of the Usher syndrome type 1F (Ush1F) to chromosome 10