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Longer titles found: Norman–Roberts syndrome (view)

searching for Roberts syndrome 6 found (27 total)

alternate case: roberts syndrome

Microlissencephaly (2,660 words) [view diff] exact match in snippet view article find links to article

clinical picture into 4 types: Microlissencephaly Type A or Norman-Roberts syndrome (NRS): a microlissencephaly with thick cortex without infratentorial
Lissencephaly (2,526 words) [view diff] exact match in snippet view article find links to article
Muscle-eye-brain disease (MEB) ( 253280) Other types LIS2: Norman-Roberts syndrome (mutation of reelin gene, 257320) LIS3: TUBA1A, 611603 LISX2: ARX,
ZWINT (814 words) [view diff] exact match in snippet view article find links to article
D, Ascoli C, Ried T, Vezzoni P (Apr 2004). "Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes"
ZW10 (1,258 words) [view diff] exact match in snippet view article find links to article
Musio A, Mariani T, Montagna C, et al. (2004). "Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes"
Reelin (15,611 words) [view diff] exact match in snippet view article find links to article
cerebellar hypoplasia classed as a microlissencephaly called Norman-Roberts syndrome. The mutations disrupt splicing of the RELN mRNA transcript, resulting
Wladimir Wertelecki (4,105 words) [view diff] case mismatch in snippet view article find links to article
Washington, D.C., Scientific Publication No. 460 (1984). Wertelecki, W.:  Roberts Syndrome.  Birth Defects Encyclopedia, 3rd Edition, Buyse, M.L., Editor. Blackwell/Year