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American Journal of Medical Genetics. Part A|May 24, 2006
Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profilesMelissa Z Antoneli, Sthella Zanchetta, Neivo L Zorzetto, et al.American Journal of Medical Genetics. Part A|May 24, 2006
Autosomal dominant atretic cephalocele with phenotype variability: report of a Brazilian family with six affected in four generationsD R Carvalho, L R Giuliani, G N Simão, et al.American Journal of Medical Genetics. Part A|August 15, 2006
Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiencyL Williamson, W Arlt, C Shackleton, et al.American Journal of Medical Genetics. Part A|March 2, 2006
Arithmetic difficulties in females with the fragile X premutationAve M Lachiewicz, Deborah V Dawson, Gail A Spiridigliozzi, et al.American Journal of Medical Genetics. Part A|June 14, 2006
Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologiesCheryl Shuman, Adam C Smith, Leslie Steele, et al.American Journal of Medical Genetics. Part A|June 14, 2006
Growth hormone therapy and scoliosis in patients with Prader-Willi syndromeT Nagai, K Obata, T Ogata, et al.American Journal of Medical Genetics. Part A|July 14, 2006
The molecular etiologies and associated phenotypes of amelogenesis imperfectaJ Timothy WrightAmerican Journal of Medical Genetics. Part A|September 27, 2006
SIX3 mutations with holoprosencephalyLucilene Arilho Ribeiro, Kenia B El-Jaick, Maximilian Muenke, et al.American Journal of Medical Genetics. Part A|September 27, 2006
Holoprosencephaly-like phenotype: clinical and genetic perspectivesA Richieri-Costa, Lucilene Arilho RibeiroAmerican Journal of Medical Genetics. Part A|September 27, 2006
Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotypeA Richieri-Costa, Lucilene Arilho RibeiroPageof 928