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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
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12
the male phenotype in osteopathia striata congenita with cranial sclerosis.pdf
the male phenotype in osteopathia striata congenita with cranial sclerosis
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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
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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
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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
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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
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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
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6
A Case Study of a Preadolescent With Osteopathia Striata With Cranial Sclerosis.[2017][J Pediatr Health Care][10.1016j.pedhc.2017.01.003].pdf
A Case Study of a Preadolescent With Osteopathia Striata With Cranial Sclerosis.[2017][J Pediatr Health Care][10.1016j.pedhc.2017.01.003]
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