Smith-Lemli-Opitz syndrome: clinical and biochemical findings in Brazilian patients. Scalco et al. Genetics and Molecular Biology (this issue) | Genet. mol. biol;Genet. mol. biol;29(3): 437-438, 2006. | LILACS

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Smith-Lemli-Opitz syndrome: clinical and biochemical findings in Brazilian patients. Scalco et al. Genetics and Molecular Biology (this issue)

Opitz, John M.

Affiliation

Opitz, John M; University of Utah School of Medicine. Human Genetics, Pathology, Obstetric & Gynecology. Salt Lake City. US

Genet. mol. biol ; Genet. mol. biol;29(3): 437-438, 2006.

Article in En | LILACS | ID: lil-450275

Responsible library: BR26.1

Subject(s)

Humans; Abnormalities, Multiple; Eye Abnormalities; Gene Frequency; Smith-Lemli-Opitz Syndrome; Brazil

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Full text: 1 Index: LILACS Main subject: Abnormalities, Multiple / Eye Abnormalities / Smith-Lemli-Opitz Syndrome / Gene Frequency Type of study: Diagnostic_studies Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Genet. mol. biol Journal subject: GENETICA Year: 2006 Type: Article

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Full text: 1 Index: LILACS Main subject: Abnormalities, Multiple / Eye Abnormalities / Smith-Lemli-Opitz Syndrome / Gene Frequency Type of study: Diagnostic_studies Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Genet. mol. biol Journal subject: GENETICA Year: 2006 Type: Article