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Jennifer Kirkham

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American Journal of Human Genetics|February 10, 2009

Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.

American Journal of Human Genetics|August 21, 2012

Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.

Community Dental Health|April 10, 2004

Developing explanatory models of health inequalities in childhood dental cariesCynthia M Pine, Pauline M Adair, Poul Erik Petersen, et al.

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Search research articles

Showing results (61-70 of 63) with videos related to

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You have reached the last page of results.This site can display upto 63 results.

American Journal of Human Genetics|February 10, 2009

Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.

American Journal of Human Genetics|August 21, 2012

Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.

Community Dental Health|April 10, 2004

Developing explanatory models of health inequalities in childhood dental cariesCynthia M Pine, Pauline M Adair, Poul Erik Petersen, et al.

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