Facial and oral structures: molecular perspectives, October 22-23, 2005COHEN, M. Michael.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, issn 1552-4825, 197 p.Conference Proceedings

Looking différent : Understanding diversity in facial formBRUGMANN, S. A; KIM, J; HELMS, J. A et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2521-2529, issn 1552-4825, 9 p.Conference Paper

Molecular basis of human dentin diseasesMACDOUEALL, Mary; JUAN DONG; ACEVEDO, Ana Carolina et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2536-2546, issn 1552-4825, 11 p.Conference Paper

The genetic basis of tooth development and dental defectsTHESLEFF, Irma.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2530-2535, issn 1552-4825, 6 p.Conference Paper

The molecular etiologies and associated phenotypes of amelogenesis imperfectaWRIGHT, J. Timothy.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2547-2555, issn 1552-4825, 9 p.Conference Paper

SIX3 mutations with holoprosencephalyARILHO RIBEIRO, Lucilene; EL-JAICK, Kenia B; MUENKE, Maximilian et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2577-2583, issn 1552-4825, 7 p.Conference Paper

Hutchinson-gilford progeria syndrome : Review of the phenotypeHENNEKAM, Raoul C. M.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2603-2624, issn 1552-4825, 22 p.Conference Paper

A newly recognized polyosteolysis/hyperostosis syndromeKANTAPUTRA, Piranit N; LIMWONGSE, Chanin; KOOLVISOOT, Ajchara et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2640-2645, issn 1552-4825, 6 p.Conference Paper

Clinical dividends from the molecular genetic diagnosis of craniosynostosisWILKIE, Andrew O. M; BOCHUKOVA, Elena G; O'ROURKE, Anthony W et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2631-2639, issn 1552-4825, 9 p.Conference Paper

Craniofacial and dental phenotype of smith-magenis syndromeTOMONA, Natalia; SMITH, Ann C. M; GUADAGNINI, Jean Pierre et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2556-2561, issn 1552-4825, 6 p.Conference Paper

Holoprosencephaly-like phenotype : Clinical and genetic perspectivesRICHIERI-COSTA, A; ARILHO RIBEIRO, Lucilene.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2587-2593, issn 1552-4825, 7 p.Conference Paper

The new bone biology : Pathologic, molecular, and clinical correlatesCOHEN, M. Michael.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2646-2706, issn 1552-4825, 61 p.Conference Paper

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populationsAVILA, Joseph R; JEZEWSKI, Peter A; VIEIRA, Alexandre R et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2562-2570, issn 1552-4825, 9 p.Conference Paper

GLI2 mutations in four Brazilian patients : How wide is the phenotypic spectrum?RAHIMOV, Fedik; ARILHO RIBEIRO, Lucilene; DE MIRANDA, Eziquiel et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2571-2576, issn 1552-4825, 6 p.Conference Paper

Patched mutations and hairy skin patches : A new sign in gorlin syndromeWILSON, Louise C; AJAYI-OBE, Ekundayo; BERNHARD, Birgitta et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2625-2630, issn 1552-4825, 6 p.Conference Paper

Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex : Association with an 1 soil. 3 deletionKANTAPUTRA, Piranit N; LIMWONGSE, Chanin; TOCHAREONTANAPHOL, Chintana et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2598-2602, issn 1552-4825, 5 p.Conference Paper

Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotypeRICHIERI-COSTA, A; ARILHO RIBEIRO, Lucilene.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2594-2597, issn 1552-4825, 4 p.Conference Paper

PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRIARILHO RIBEIRO, Lucilene; MURRAY, Jeffrey C; RICHIERI-COSTA, Antonio et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2584-2586, issn 1552-4825, 3 p.Conference Paper