I guess no one can say anything about this specific science question. (I am surprised it is a hard one, at all)
If so, how could anyone still insist the evolution is so correct that even the Genesis creation "must" not be real?
Having unanswered questions in a theory is not the same as having evidence to show a theory is wrong.
Creationism has data that can't be there if creationism were true. Therefore it is wrong.
Not knowing the evolutionary origin of every organ does not mean that organ doesn't have one. Thinking it does is simply poor logic.
When you have one of these "how did it happen" questions, I suggest you always go to PubMed before you post.
I did find this:
"1: Biol Rev Camb Philos Soc. 1990 Aug;65(3):277-373.
Development and evolutionary origins of vertebrate skeletogenic and odontogenic tissues.
Smith MM, Hall BK.
Unit of Anatomy in Relation to Dentistry, United Medical School, Guy's Hospital,
London Bridge, U.K.
This review deals with the following seven aspects of vertebrate skeletogenic and odontogenic tissues. 1. The evolutionary sequence in which the tissues appeared amongst the lower craniate taxa. 2. The topographic association between skeletal (cartilage, bone) and dental (dentine, cement, enamel) tissues in the
oldest vertebrates of each major taxon. 3. The separate developmental origin of the exo- and endoskeletons. 4. The neural-crest origin of cranial skeletogenic
and odontogenic tissues in extant vertebrates. 5. The neural-crest origin of trunk dermal skeletogenic and odontogenic tissues in extant vertebrates. 6. The
developmental processes that control differentiation of skeletogenic and odontogenic tissues in extant vertebrates. 7. Maintenance of developmental
interactions regulating skeletogenic/odontogenic differentiation across vertebrate taxa. We derive twelve postulates, eight relating to the earliest vertebrate skeletogenic and odontogenic tissues and four relating to the development of these tissues in extant vertebrates and extrapolate the developmental data back to the evolutionary origin of vertebrate skeletogenic and odontogenic tissues. The conclusions that we draw from this analysis are as follows. 8. The dermal exoskeleton of thelodonts, heterostracans and
osteostracans consisted of dentine, attachment tissue (cement or bone), and bone. 9. Cartilage (unmineralized) can be inferred to have been present in heterostracans and osteostracans, and globular mineralized cartilage was present in Eriptychius, an early Middle Ordovician vertebrate unassigned to any established group, but assumed to be a stem agnathan. 10. Enamel and possibly also enameloid was present in some early agnathans of uncertain affinities. The majority of dentine tubercles were bare. 11. The contemporaneous appearance of cellular and acellular bone in eterostracans and osteostracans during the
Ordovician provides no clue as to whether one is more primitive than the other. 12. We interpret aspidin as being developmentally related to the odontogenic
attachment tissues, either closer to dentine or a form of cement, rather than as derived from bone. 13. Dentine is present in the stratigraphically oldest (Cambrian) assumed vertebrate fossils, at present some only included as Problematica, and is cladistically primitive, relative to bone. 14. The first vertebrate exoskeletal skeletogenic ability was expressed as denticles of dentine. 15. Dentine, the bone of attachment associated with dentine, the basal bone to which dermal denticles are fused and cartilage of the Ordovician agnathan dermal exoskeleton were all derived from the neural crest and not from mesoderm. Therefore the earliest vertebrate skeletogenic/odontogenic tissues
were of neural-crest origin."
There are also papers looking at the origin of some of the specific proteins involved in the formation of bone.
1: J Exp Zoolog B Mol Dev Evol. 2006 May 15;306(3):295-316.
Evolutionary genetics of vertebrate tissue mineralization: the origin and
evolution of the secretory calcium-binding phosphoprotein family.
Kawasaki K, Weiss KM.
Department of Anthropology, Pennsylvania State University, University Park,
Pennsylvania 16802, USA.
Three principal mineralized tissues are present in teeth; a highly mineralized surface layer (enamel or enameloid), body dentin, and basal bone. Similar tissues have been identified in the dermal skeleton of Paleozoic jawless
vertebrates, suggesting their ancient origin. These dental tissues form on
protein matrix and their mineralization is controlled by distinctive proteins.
We have shown that many secretory calcium-binding phosphoproteins (SCPPs) are
involved in tetrapod tissue mineralization. These SCPPs all originated from the
common ancestral gene SPARCL1 (secreted protein, acidic, cysteine-rich like 1)
that initially arose from SPARC. The SCPP family also includes a bird eggshell
matrix protein, mammalian milk casein, and salivary proteins. The eggshell SCPP
plays crucial roles in rigid eggshell production, milk SCPPs in efficient
lactation and in the evolution of complex dentition, and salivary SCPPs in
maintaining tooth integrity. A comparative analysis of the mammalian, avian, and
amphibian genomes revealed a tandem duplication history of the SCPP genes in
tetrapods. Although these tetrapod SCPP genes are fewer in teleost genomes,
independent parallel duplication has created distinct SCPP genes in this
lineage. These teleost SCPPs are also used for enameloid and dentin
mineralization, implying essential roles of SCPPs for dental tissue
mineralization in osteichthyans. However, the SCPPs used for tetrapod enamel and
teleost enameloid, as well as tetrapod dentin and teleost dentin, are all
different. Thus, the evolution of vertebrate mineralized tissues seems to be
explained by phenogenetic drift: while mineralized tissues are retained during
vertebrate evolution, the underlying genetic basis has extensively drifted.