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Distinctive Phenotype in 9 Patients with Deletion of Chromosome 1q24-q25
Reports of individuals with deletions of 1q24→q25 share common features of prenatal onset growth deficiency, microcephaly, small hands and feet, dysmorphic face and severe cognitive deficits. We report nine individuals with 1q24q25 deletions, who show distinctive features of a clinically recognizabl...
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Main Authors: | , , , , , , , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2011
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3109510/ https://ncbi.nlm.nih.gov/pubmed/21548129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.34049 |
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