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Mosaic partial trisomy 17q2.

Examination of an infant born after prenatal diagnosis of mosaic partial trisomy 17q2 showed the unique phenotypic features of this chromosomal abnormality, that is, frontal bossing, large mouth, brachyrhizomelia, and hexadactyly. Amniocentesis was performed because of polyhydramnios and ultrasound...

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Detalles Bibliográficos
Publicado en:J Med Genet
Autores principales: King, P A, Ghosh, A, Tang, M
Formato: Artigo
Lenguaje:Inglês
Publicado: BMJ Publishing Group 1991
Materias:
Acceso en línea:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015800/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1956067/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.9.641
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