An additional family with association of hereditary thrombocytosis and transverse limb deficiency: confirmation of a rare clinical spectrum.
Data(s) |
2012
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Identificador |
http://serval.unil.ch/?id=serval:BIB_4E695D65DB45 isbn:1552-4833 (Electronic) pmid:23165915 doi:10.1002/ajmg.a.35656 isiid:000311401800032 |
Idioma(s) |
en |
Fonte |
American Journal of Medical Genetics. Part A, vol. 158A, no. 12, pp. 3211-3213 |
Tipo |
info:eu-repo/semantics/article article |