PMID: 3746837Aug 1, 1986Paper

Robinow syndrome without mesomelic 'brachymelia': a report of five cases

Journal of Medical Genetics
M D BainJ Burn

Abstract

A family is described in which the father and his two children had Robinow syndrome, but with no consistent brachymelia or dwarfism. Two further sporadic cases are described, one with rhizomelic brachymelia and dwarfism and the other with generalised shortening of the limbs. An attempt is also made to distinguish between the phenotype of autosomal dominant and recessive cases on the basis of the familial cases in this paper and other reported cases.

References

Apr 1, 1979·Journal of Medical Genetics·R S Wadia
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Jun 1, 1969·American Journal of Diseases of Children·M RobinowH D Smith
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Jul 1, 1982·American Journal of Diseases of Children·R J ShprintzenE J Sidoti

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Citations

Jun 1, 1989·European Journal of Pediatrics·D GlaserW Lenz
Aug 1, 1992·European Journal of Pediatrics·D F SchorderetM A Morris
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Oct 16, 2010·American Journal of Medical Genetics. Part a·Marco CastoriPaola Grammatico
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Feb 19, 2021·Journal of the American Society of Nephrology : JASN·Miguel VerbitskyAli G Gharavi
Sep 18, 2015·International Journal of Clinical Pediatric Dentistry·Cristalle Soman, Ashok Lingappa

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