Literature DB >> 14013338

[Familial nephropathy with bone and chorioretinal involvement].

B ANTOINE, S BRAUN-VALLON, D PERRIN, J P DUNOD, A RYCKEWAERT.   

Abstract

Entities:  

Keywords:  KIDNEY DISEASES; OSTEOSCLEROSIS; RETINITIS PIGMENTOSA

Mesh:

Year:  1963        PMID: 14013338

Source DB:  PubMed          Journal:  J Urol Nephrol (Paris)        ISSN: 0021-8200


× No keyword cloud information.
  2 in total

1.  Night blindness, characteristic facies, and skeletal abnormalities in two brothers.

Authors:  A G Hunter; D R Thompson; M H Reed; A G Macrodimitris
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

2.  Hereditary renal-retinal dysplasia.

Authors:  V Godel; A Iaina; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1980-10-15       Impact factor: 2.379

  2 in total

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