An additional family with association of hereditary thrombocytosis and transverse limb deficiency: confirmation of a rare clinical spectrum.


Autoria(s): Graziano C.; David M.; Magini P.; Superti-Furga A.; Seri M.
Data(s)

2012

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