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American Journal of Medical Genetics. Part A|September 18, 2008
High prevalence of orofacial clefts in Shanxi Province in northern China, 2003-2004Zhiwen Li, Aiguo Ren, Jianmeng Liu, et al.American Journal of Medical Genetics. Part A|September 18, 2008
Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotypeSarah T South, Heidi Whitby, Teresa Maxwell, et al.American Journal of Medical Genetics. Part A|August 15, 2009
DeltaNp63 knockdown mice: A mouse model for AEC syndromeMaranke I Koster, Barbara Marinari, Aimee S Payne, et al.American Journal of Medical Genetics. Part A|August 15, 2009
Approach towards a new classification for ectodermal dysplasias: integration of the clinical and molecular knowledgeJohn J DiGiovanna, Manuela Priolo, Peter ItinAmerican Journal of Medical Genetics. Part A|July 18, 2009
Mosaic trisomy 1q: The longest surviving caseChirag Patel, Graham Hardy, Phillip Cox, et al.American Journal of Medical Genetics. Part A|April 9, 2009
Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromesKaren W Gripp, Elizabeth Hopkins, Chana Vinkler, et al.American Journal of Medical Genetics. Part A|April 9, 2009
Vertebral fusion in a patient with supernumerary-der(22)t(11;22) syndromeMitsuo Toyoshima, Chihiro Yonee, Yoshihiro Maegaki, et al.American Journal of Medical Genetics. Part A|April 9, 2009
aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsyAaron Theisen, Jill A Rosenfeld, Sandra A Farrell, et al.American Journal of Medical Genetics. Part A|April 9, 2009
NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafnessKerry K Brown, Fowzan S Alkuraya, Michael Matos, et al.American Journal of Medical Genetics. Part A|November 14, 2008
Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathyMariet Elting, Ariana Kariminejad, Marie-Louise de Sonnaville, et al.Pageof 929