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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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M R Eccles

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International Journal of Oncology|May 4, 2012

PAX2 is an antiapoptotic molecule with deregulated expression in medulloblastomaM C Burger, D P Brucker, P Baumgarten, et al.

Cancer Research|June 1, 1992

A third Wilms' tumor locus on chromosome 16qM A Maw, P E Grundy, L J Millow, et al.

European Journal of Human Genetics : EJHG|November 28, 2000

PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicismJ Amiel, S Audollent, D Joly, et al.

The Journal of Pathology|April 27, 2013

Biallelic DICER1 mutations occur in Wilms tumoursM K Wu, N Sabbaghian, B Xu, et al.

American Journal of Human Genetics|April 1, 1997

Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutationsL A Schimmenti, H E Cunliffe, L A McNoe, et al.

Scientific Reports|May 11, 2017

An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutationsC Stayner, C A Poole, S R McGlashan, et al.

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Search research articles

Showing results (41-50 of 46) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 46 results.

International Journal of Oncology|May 4, 2012

PAX2 is an antiapoptotic molecule with deregulated expression in medulloblastomaM C Burger, D P Brucker, P Baumgarten, et al.

Cancer Research|June 1, 1992

A third Wilms' tumor locus on chromosome 16qM A Maw, P E Grundy, L J Millow, et al.

European Journal of Human Genetics : EJHG|November 28, 2000

PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicismJ Amiel, S Audollent, D Joly, et al.

The Journal of Pathology|April 27, 2013

Biallelic DICER1 mutations occur in Wilms tumoursM K Wu, N Sabbaghian, B Xu, et al.

American Journal of Human Genetics|April 1, 1997

Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutationsL A Schimmenti, H E Cunliffe, L A McNoe, et al.

Scientific Reports|May 11, 2017

An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutationsC Stayner, C A Poole, S R McGlashan, et al.

Pageof 5