₁₁Michel Vekemans

Summary for 2007 [at-glance overview of Michel Vekemans work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Michel Vekemans. According to available data, in 2007 Michel Vekemans published at least 11 articles. This work was completed in collaboration with several authors including Attié-Bitach, Tania and Encha-Razavi, Ferechte. Many other authors have collaborated with Michel Vekemans as well. There is no information about the funding or the grants awarded to support this work.

Michel Vekemans has rank 11 when compared to all other authors using the keyword Abnormalities, Multiple. Analysis of the article abstracts and the titles suggests that Michel Vekemans professional interests are focused around "supporting autosomal recessive", "onset thyroid function" and "sodium iodide symporter". These might also be referred to as "matthew-wood syndrome", "joubert syndrome" or "meckel syndrome". Statistical analysis shows that Michel Vekemans's writing is likely to contains terms "syndrome", "mutations", "gene", "identified", "js" and "mks3".

Unfortunately, there is not enough information to establish Michel Vekemans affiliation. Luckily, several email addresses are on file.

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Alternative names (1) [other authors with names similar to Michel Vekemans]

• ₉₄Vekemans, M

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