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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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Pubblicato in:J Med Genet
Autori principali: King, P A, Ghosh, A, Tang, M
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Publishing Group 1991
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Accesso online: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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