Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome
- 1 March 2005
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 76 (3), 493-504
- https://doi.org/10.1086/428679
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndromeNature Genetics, 2004
- Antenatal renal sonographic anomalies and postnatal follow‐up of renal involvement in Bardet–Biedl syndromeUltrasound in Obstetrics & Gynecology, 2004
- The oligogenic properties of Bardet-Biedl syndromeHuman Molecular Genetics, 2004
- Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2American Journal of Human Genetics, 2003
- A novel locus for Meckel-Gruber syndrome, MKS3 , maps to chromosome 8q24Human Genetics, 2002
- Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeNature Genetics, 2002
- A Gene for Meckel Syndrome Maps to Chromosome 11q13American Journal of Human Genetics, 1998
- The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24Nature Genetics, 1995
- Cystic kidney dysplasia and polydactyly in 3 sibs with Bardet‐Biedl syndromeAmerican Journal of Medical Genetics, 1992
- The Goldston Syndrome: Report of a CasePediatric Pathology, 1989