Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
about
New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population surveyPhenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivityBrain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS)Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genesIntrafamilial variation of the phenotype in Bardet-Biedl syndrome.Deletion of myosin VI causes slow retinal optic neuropathy and age-related macular degeneration (AMD)-relevant retinal phenotype.Genetic basis of Joubert syndrome and related disorders of cerebellar development.Retinitis pigmentosa, pigmentary retinopathies, and neurologic diseases.Clinical pathology and retinal vascular structure in the Bardet-Biedl syndromeNeuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes.Cerebellar vermis hypoplasia in a patient with Bardet-Biedl syndrome.Full-field electroretinograms in individuals with the Laurence-Mood-Bardet-Biedl syndrome.Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome.Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotype.Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome.
P2860
Q24681777-A963CBED-1DAF-4A49-B336-CE41569F0306Q28505984-75F0C000-3A90-4BC6-A4B1-78DDAB3970B2Q33973018-2BC74B6A-46CF-450C-83DC-41F875DE52FFQ35221428-136139E4-E3A6-4B48-B04C-B7AC8DF43F8FQ35300227-2FE33D1F-268E-4CC4-B81B-09C0C54D527AQ36074569-D9F7A098-7990-4AE6-86E0-FB6F6BCF4211Q36294694-D18AC75A-3011-4728-BABA-0C0A5BA32A16Q36575018-D41BA0B8-E7F5-40A8-8214-270964C11AA9Q37310151-CB209B68-392A-4A60-9803-2A0FA266AEE4Q38430972-1FE48C0D-AB31-4B3B-AA88-B78619CC53AFQ38522307-CA8F7A77-AC42-4519-BCD0-96FAEB93CDC1Q38530513-78E543FF-45AA-4E28-8945-82B8CDCD1AB4Q38530516-E04144BF-6308-4493-8221-B80FB6489441Q38531121-855F3C23-4322-4A6C-A61C-BC11AD62B912Q38534241-0A189C52-5FB8-4A24-943C-EAA06CA35B1E
P2860
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
@en
type
label
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
@en
prefLabel
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
@en
P2093
P1433
P1476
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
@en
P2093
Rizzo JF 3rd
P304
P356
10.1016/S0161-6420(86)33546-2
P577
1986-11-01T00:00:00Z