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American Journal of Medical Genetics. Part A|October 17, 2007
Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardationKatarzyna Borg, Beata Nowakowska, Ewa Obersztyn, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Genotype/phenotype correlations in two patients with 12q subtelomere deletionsDmitriy M Niyazov, Zafar Nawaz, April N Justice, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotypeIngrid Van de Laar, Dennis Dooijes, Lies Hoefsloot, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
The emotional effects of genetic diseases: implications for clinical geneticsMarion McAllister, Linda Davies, Katherine Payne, et al.
American Journal of Medical Genetics. Part A|October 30, 2007
Two siblings with an unusual nasal malformation: further instances of craniorhiny?Melissa M Lees, Loshan Kangesu, Per Hall, et al.
American Journal of Medical Genetics. Part A|October 30, 2007
Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patientsJulie C Sapp, Joyce T Turner, Jiddeke M van de Kamp, et al.
American Journal of Medical Genetics. Part A|November 14, 2007
Does single umbilical artery (SUA) predict any type of congenital defect? Clinical-epidemiological analysis of a large consecutive series of malformed infantsMaría Luisa Martínez-Frías, Eva Bermejo, Elvira Rodríguez-Pinilla, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Complementary and alternative medicine (CAM) in geneticsBruce A Buehler
American Journal of Medical Genetics. Part A|November 15, 2007
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNAZöe Powis, Sung-Hae L Kang, M Lance Cooper, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findingsDavid Chitayat, Patrick Shannon, Sarah Keating, et al.
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