Bardet-Biedl syndrome - Aspects of nephro-urology and human genetics;Bardet-Biedl-syndrom: Nephrourologische und humangenetishe aspekte

Klinische Padiatrie

Volumn 213, Issue 1, 2001, Pages 8-12

  Bruhl P ^a   Schwanitz, G ^b   Mallmann, R ^a   Muller S C ^a   Raff, R ^b  

^a UNIVERSITY OF BONN   (Germany)

^b Institut für Humangenetik   (Germany)

Author keywords

Bardet Biedl syndrome; Endocrinology; Human genetics; Imaging renal masses; Nephrology; Urology

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BARDET BIEDL SYNDROME; BLINDNESS; GENE LOCUS; GENETIC HETEROGENEITY; HUMAN; HUMAN TISSUE; HYPOGONADISM; MENTAL DEFICIENCY; OBESITY; POLYDACTYLY; RETINA DEGENERATION; SYNDROME DELINEATION;

ADOLESCENT; ADULT; AGE FACTORS; BARDET-BIEDL SYNDROME; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; IMMUNOSUPPRESSIVE AGENTS; INFANT; INFANT, NEWBORN; KIDNEY DISEASES; KIDNEY TRANSPLANTATION; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; OBESITY; PHENOTYPE; PROGNOSIS;

EID: 0035122903     PISSN: 03008630     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-11265     Document Type: Article

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42. A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31