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. 1994 Oct;55(4):853–855.

Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.

F Gurrieri, M Genuardi, P Chiurazzi, G Gillessen-Kaesbach, G Neri
PMCID: PMC1918293  PMID: 7942863

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Akita S., Kuratomi H., Abe K., Harada N., Mukae N., Niikawa N. EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3). Clin Dysmorphol. 1993 Jan;2(1):62–67. [PubMed] [Google Scholar]
  2. Chi D. D., Hing A. V., Helms C., Steinbrueck T., Mishra S. K., Donis-Keller H. Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and pro alpha 2 (I) collagen (COL1A2). Hum Mol Genet. 1992 May;1(2):135–135. doi: 10.1093/hmg/1.2.135. [DOI] [PubMed] [Google Scholar]
  3. 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]
  4. Grzeschik K. H., Tsui L. C., Green E. D. Report and abstracts of the First International Workshop on Human Chromosome 7 Mapping 1993. Cytogenet Cell Genet. 1994;65(1-2):52–73. [PubMed] [Google Scholar]
  5. Lathrop G. M., Lalouel J. M. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet. 1984 Mar;36(2):460–465. [PMC free article] [PubMed] [Google Scholar]
  6. 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]
  7. Ott J. A computer program for linkage analysis of general human pedigrees. Am J Hum Genet. 1976 Sep;28(5):528–529. [PMC free article] [PubMed] [Google Scholar]
  8. 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]
  9. Rivera H., Sanchez-Corona J., Burgos-Fuentes V. R., Melendez-Ruiz M. J. Deletion of 7q22 and ectrodactyly. Genet Couns. 1991;2(1):27–31. [PubMed] [Google Scholar]
  10. Scherer S. W., Poorkaj P., Allen T., Kim J., Geshuri D., Nunes M., Soder S., Stephens K., Pagon R. A., Patton M. A. Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1. Am J Hum Genet. 1994 Jul;55(1):12–20. [PMC free article] [PubMed] [Google Scholar]
  11. Tajara E. H., Varella-Garcia M., Gusson A. C. Interstitial long-arm deletion of chromosome 7 and ectrodactyly. Am J Med Genet. 1989 Feb;32(2):192–194. doi: 10.1002/ajmg.1320320212. [DOI] [PubMed] [Google Scholar]
  12. Weissenbach J., Gyapay G., Dib C., Vignal A., Morissette J., Millasseau P., Vaysseix G., Lathrop M. A second-generation linkage map of the human genome. Nature. 1992 Oct 29;359(6398):794–801. doi: 10.1038/359794a0. [DOI] [PubMed] [Google Scholar]

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