38
genetic and molecular insights into genotype-phenotype relationships in osteopathia striata with cranial sclerosis (oscs) through the analysis of n.pdf
genetic and molecular insights into genotype-phenotype relationships in osteopathia striata with cranial sclerosis (oscs) through the analysis of n
12
the male phenotype in osteopathia striata congenita with cranial sclerosis.pdf
the male phenotype in osteopathia striata congenita with cranial sclerosis
6
severe osteopathia striata with cranial sclerosis in a female case with whole wtx gene deletion.pdf
severe osteopathia striata with cranial sclerosis in a female case with whole wtx gene deletion
6
unclassified sclerosing bone dysplasia with osteopathia striata, cranial sclerosis, metaphyseal undermodeling, and bone fragility.pdf
unclassified sclerosing bone dysplasia with osteopathia striata, cranial sclerosis, metaphyseal undermodeling, and bone fragility
5
a novel wtx mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma.pdf
a novel wtx mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma
7
osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region xq11.2.pdf
osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region xq11.2
6
two novel lt;em gt;wtx lt;em gt; mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis.pdf
two novel
5
male child with somatic mosaic osteopathia striata with cranial sclerosis caused by a novel pathogenic amer1 frameshift mutation.[2017][am j med ge.pdf
male child with somatic mosaic osteopathia striata with cranial sclerosis caused by a novel pathogenic amer1 frameshift mutation.[2017][am j med ge

向豆丁求助:有没有osteopathia?

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