A gene for usher syndrome type I (USH1A) maps to chromosome 14q

Genomics

Volumn 14, Issue 4, 1992, Pages 979-987

  Kaplan, J ^a,c   Gerber, S ^a,c   Bonneau, D ^a,c   Rozet, J M ^a,c   Delrieu, O ^a,c   Briard, M L ^a,c   Dollfus, H ^a,c   Ghazi, I ^b,c   Dufier, J L ^b,c   Frezal J ^a,c   Munnich, A ^a,c  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b University of Poitiers   (France)

^c Hopital Laennec   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 14Q; CLINICAL ARTICLE; DNA PROBE; FAMILY STUDY; FEMALE; FRANCE; GENE; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; MALE; NORMAL HUMAN; USHER SYNDROME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 14; FEMALE; HEARING DISORDERS; HUMAN; LINKAGE (GENETICS); MALE; PEDIGREE; RETINITIS PIGMENTOSA; SYNDROME;

EID: 0027058632     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/S0888-7543(05)80120-X     Document Type: Article

References (21)

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3. Usher syndrome: Definition and estimate of prevalence from two high-risk populations
4. Linkage mapping of a mouse gene, “iv,” that controls left-right asymmetry of the heart and viscera
5. Possible genetic heterogenity of Usher syndrome type 2: A family unlinked to chromosome 1q markers
6. Usher's syndrome: Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity
7. Retinitis pigmentosa with congenital deafness with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases A clinical and genetico-statistical study
8. Abnormal sperm and photoreceptor axonemes in Usher's syndrome
9. Clinical and genetic heterogeneity in retinitis pigmentosa
10. Usher syndrome type I is not linked to D1S81 (pTHH33): Evidence for genetic heterogeneity
11. Localization of Usher syndrome type II to chromosome 1q
12. Kartagener syndrome and deafmutism: An unusual association
13. Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
14. Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q
15. Innervation densities of inner and outer hair cells of the human organ of Corti
16. Frequent recombination is observed in the distal end of the long arm of chromosome 14
17. Dystrophia retinae pigmentosa-dysacusis syndrome: A study of the Usher or Hallgren syndrome
18. Removal of repeat sequences from hybridization probes
19. Histopathology of the inner ear in User's syndrome as observed by light and electron microscopy
20. On the inheritance of retinitis pigmentosa with notes of cases