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A male infant with a deletion of 9p and concomitant duplication of 4q: 46,XY, der(9)t(4;9)(q27;p24), is described. Parental chromosome analysis showed a balanced maternal translocation. To our knowledge, the above cytogenetic and clinical abnormaliti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::84b7a9679e789a9ac79fa4b1f1ef1fd6
http://europepmc.org/abstract/med/10526659
http://europepmc.org/abstract/med/10526659