837573

Source:http://linkedlifedata.com/resource/pubmed/id/837573

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0009807, umls-concept:C0030705, umls-concept:C0039082, umls-concept:C0678226, umls-concept:C1442161, umls-concept:C1858460
pubmed:issue	3
pubmed:dateCreated	1977-4-28
pubmed:abstractText	Deletion of the short arm of chromosome 9, derived from a 3:1 meiotic segregation in the mother, carrier of a balanced 9/15 translocation, was found in a 3-year-old female. Severe psychomotor retardation with delayed speech, brachicephaly, flat occiput hypertelorism and long upper lip were the main signs in the girl.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0009-9163
pubmed:author	pubmed-author:BergamoFF, pubmed-author:CrosatoFF, pubmed-author:FrancesconiDD, pubmed-author:PasqualFF, pubmed-author:ZuffardiOO
pubmed:issnType	Print
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	219-23
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:837573-Abnormalities, Multiple, pubmed-meshheading:837573-Child, Preschool, pubmed-meshheading:837573-Chromosome Aberrations, pubmed-meshheading:837573-Chromosome Deletion, pubmed-meshheading:837573-Chromosomes, Human, 13-15, pubmed-meshheading:837573-Chromosomes, Human, 6-12 and X, pubmed-meshheading:837573-Female, pubmed-meshheading:837573-Humans, pubmed-meshheading:837573-Meiosis, pubmed-meshheading:837573-Psychomotor Disorders, pubmed-meshheading:837573-Translocation, Genetic
pubmed:year	1977
pubmed:articleTitle	The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction.
pubmed:publicationType	Journal Article, Case Reports