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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1998 Dec;35(12):1054–1055. doi: 10.1136/jmg.35.12.1054-c

Genotypic/phenotypic heterogeneity of Kenny-Caffey syndrome.

M A Sabry, M Zaki, A Shaltout
PMCID: PMC1051528  PMID: 9863613

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Selected References

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

  1. Hershkovitz E., Shalitin S., Levy J., Leiberman E., Weinshtock A., Varsano I., Gorodischer R. The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patients. Isr J Med Sci. 1995 May;31(5):293–297. [PubMed] [Google Scholar]
  2. Sabry M. A., Zaki M., Abul Hassan S. J., Ramadan D. G., Abdel Rasool M. A., al Awadi S. A., al Saleh Q. Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster. J Med Genet. 1998 Jan;35(1):31–36. doi: 10.1136/jmg.35.1.31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Tahseen K., Khan S., Uma R., Usha R., Al Ghanem M. M., Al Awadi S. A., Farag T. I. Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed. Am J Med Genet. 1997 Mar 17;69(2):126–132. [PubMed] [Google Scholar]

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