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A complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study.

We report a male infant referred with multiple congenital abnormalities consistent with the Wolf-Hirschhorn syndrome. Cytogenetic analysis showed a chromosome complement of 46,XX with a deletion of 4p15.2----4pter and its replacement by material of unknown origin. The patient was positive for a numb...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Coles, K, Mackenzie, M, Crolla, J, Harvey, J, Starr, J, Howard, F, Jacobs, P
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1992
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015991/
https://ncbi.nlm.nih.gov/pubmed/1619635
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