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searching for RNF135 7 found (11 total)

alternate case: rNF135

CRLF3 (645 words) [view diff] exact match in snippet view article find links to article

Vijfhuizen L, van der Wielen MJ, Kant SG, Breuning MH, et al. (February 2009). "RNF135 mutations are not present in patients with Sotos syndrome-like features"

EVI2B (472 words) [view diff] exact match in snippet view article find links to article

PMID 16344560. Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities

UTP6 (607 words) [view diff] exact match in snippet view article find links to article

PMID 17380155. Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities

OMG (gene) (604 words) [view diff] exact match in snippet view article

S2CID 24738309. Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities

RAB11FIP4 (617 words) [view diff] exact match in snippet view article find links to article

S2CID 13709685. Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities

Suz12 polycomb repressive complex 2 subunit pseudogene 1 (101 words) [view diff] exact match in snippet view article find links to article

L, van der Wielen MJ, Kant SG, Breuning MH, Wit JM, Losekoot M (2009). "RNF135 mutations are not present in patients with Sotos syndrome-like features"

CENTA2 (476 words) [view diff] exact match in snippet view article find links to article

S2CID 45891228. Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities