Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Chatkupt S., Speer M. C., Ding Y., Thomas M., Stenroos E. S., Dermody J. J., Koenigsberger M. R., Ott J., Johnson W. G. Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele. Am J Med Genet. 1994 Aug 1;52(1):1–4. doi: 10.1002/ajmg.1320520102. [DOI] [PubMed] [Google Scholar]
- Genuardi M., Pomponi M. G., Sammito V., Bellussi A., Zollino M., Neri G. Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1. Am J Med Genet. 1993 Nov 1;47(6):823–831. doi: 10.1002/ajmg.1320470606. [DOI] [PubMed] [Google Scholar]
- Marinoni J. C., Boyd E., Sherman S., Schwartz C. Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1. Hum Mol Genet. 1994 Aug;3(8):1355–1357. doi: 10.1093/hmg/3.8.1355. [DOI] [PubMed] [Google Scholar]
- Morey M. A., Higgins R. R. Ectro-amelia syndrome associated with an interstitial deletion of 7q. Am J Med Genet. 1990 Jan;35(1):95–99. doi: 10.1002/ajmg.1320350118. [DOI] [PubMed] [Google Scholar]
- Palmer S. E., Scherer S. W., Kukolich M., Wijsman E. M., Tsui L. C., Stephens K., Evans J. P. Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation. Am J Hum Genet. 1994 Jul;55(1):21–26. [PMC free article] [PubMed] [Google Scholar]