Back in 2006 I parodied Mark's "objection" to human evolution with "I can't believe it's not a brain", which was a reference to I can't believe it's not butter. The humor was lost on him, but the point remains 10 years later - his only objection is personal incredulity.
That's the difference between me and you, you write parody and I read genetics:
the promoter and first nine exons of SRGAP2 (large interspersed duplication of 258 kbp) ) duplicated to become SRGAP2B ~3.4 million years ago (mya). Two larger duplications later copied SRGAP2B (two larger duplications >500 kbp) to become SRGAP2C SRGAP2D ~2.4 and ~1 mya…Coinciding with the transition of Australopithecus to Homo and the beginning of neocortex expansion…the development of language (FOXP2), changes in the musculature of the jaw (MYH16), and limb and digit specializations (HACNS1). (Human-specific evolution of novel SRGAP2 genes by incomplete segmental duplication. Cell. 2012 May 11)
That's a gene(s) involved in the development of the human brain. The human brain is about twice as dense as any other apes and this genetic basis is why. You guys like to pretend it's a simple matter but there is far more involved then personal incredulity, it's the Darwinian who is arguing from ignorance which is the real meaning of 'argument from incredulity'.
A very long string of events have to happen with clock work precision to include three duplications. Then there have to be extraordinary mutations involving whole exons and amino acid sequences of considerable length. One simulation calculates how likely a gene duplication would be given no selective pressure:
In most models of the development of evolutionary novelty by gene duplication, it is implicitly assumed that a single, albeit rare, mutation to the duplicated gene can confer a new selectable property…In particular, some protein features require the participation of multiple amino acid residues (MR)...If six mutations were required then, as indicated by Figure 6, on average a population size of ∼10^22 organisms would be necessary to fix the MR feature in 10^8 generations, and a population of ∼10^30 organisms would be expected to fix the mutation in one million generations...In order for such a process to occur in vivo by gene duplication and point mutation within a hundred million generations would be expected on average to require >10^25 organisms. (Simulating evolution by gene duplication of protein features that require multiple amino acid residues Protein Science 2004)
Incredulous because this ridiculous fantasy has to be assumed?
Getting back to the SRGAP2 gene, they screened 7,137 individuals finding, 'no deletions of SRGAP2C …with rare deletions and duplications observed only in cases with intellectual disability for SRGAP2A':
a ten-year-old child with a history of seizures, attention deficit disorder, and learning disabilities. An MRI of this patient also indicates several brain malformations, including hypoplasia of the posterior body of the corpus callosum…a five-year-old girl diagnosed with West syndrome and exhibiting epileptic seizures, intellectual disability, cortical atrophy, and a thin corpus callosum…(Human-specific evolution of novel SRGAP2 genes by incomplete segmental duplication. Cell. 2012 May 11)
Which is understandable since the gene is highly conserved due to it's vital effect on brain development. They found the protein product from this gene in:
adipose, whole brain, cerebral cortex, breast, colon, heart, liver, lymph node, skeletal muscle, lung and testes…genes having highest expression level was highest in cerebral cortex followed by the testes (Cell 2011)
Why don't you write another parody because trivializing the seriousness of the subject matter appears to be your sole contribution to these boards.
Have a nice day

Mark