A mother with VCFS and unilateral dysplastic kidney and her fetus with multicystic dysplastic kidneys: additional evidence to support the association of renal malformations and VCFS

. 1998 Apr;35(4):348. doi: 10.1136/jmg.35.4.348

A mother with VCFS and unilateral dysplastic kidney and her fetus with multicystic dysplastic kidneys: additional evidence to support the association of renal malformations and VCFS.

PMCID: PMC1051299 PMID: 9598740

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Devriendt K., Moerman P., Van Schoubroeck D., Vandenberghe K., Fryns J. P. Chromosome 22q11 deletion presenting as the Potter sequence. J Med Genet. 1997 May;34(5):423–425. doi: 10.1136/jmg.34.5.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
Driscoll D. A., Budarf M. L., Emanuel B. S. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11. Am J Hum Genet. 1992 May;50(5):924–933. [PMC free article] [PubMed] [Google Scholar]
Driscoll D. A., Salvin J., Sellinger B., Budarf M. L., McDonald-McGinn D. M., Zackai E. H., Emanuel B. S. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis. J Med Genet. 1993 Oct;30(10):813–817. doi: 10.1136/jmg.30.10.813. [DOI] [PMC free article] [PubMed] [Google Scholar]
Lindsay E. A., Greenberg F., Shaffer L. G., Shapira S. K., Scambler P. J., Baldini A. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region. Am J Med Genet. 1995 Mar 27;56(2):191–197. doi: 10.1002/ajmg.1320560216. [DOI] [PubMed] [Google Scholar]
Palacios J., Gamallo C., García M., Rodríguez J. I. Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly. Am J Med Genet. 1993 Jul 1;46(6):641–646. doi: 10.1002/ajmg.1320460608. [DOI] [PubMed] [Google Scholar]