1684352

Source:http://linkedlifedata.com/resource/pubmed/id/1684352

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0000772, umls-concept:C0008059, umls-concept:C0008672, umls-concept:C0424230, umls-concept:C1442161, umls-concept:C1515568
pubmed:issue	5
pubmed:dateCreated	1992-1-29
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985062R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0019-6061
pubmed:author	pubmed-author:BankerG JGJ, pubmed-author:MurphyH SHS, pubmed-author:MurthyS KSK, pubmed-author:PatelA JAJ
pubmed:issnType	Print
pubmed:volume	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	546-9
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:1684352-Abnormalities, Multiple, pubmed-meshheading:1684352-Chromosome Aberrations, pubmed-meshheading:1684352-Chromosome Deletion, pubmed-meshheading:1684352-Chromosomes, Human, Pair 9, pubmed-meshheading:1684352-Craniofacial Dysostosis, pubmed-meshheading:1684352-Cryptorchidism, pubmed-meshheading:1684352-Humans, pubmed-meshheading:1684352-Infant, pubmed-meshheading:1684352-Karyotyping, pubmed-meshheading:1684352-Male, pubmed-meshheading:1684352-Psychomotor Disorders
pubmed:year	1991
pubmed:articleTitle	De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
pubmed:affiliation	Department of Zoology (Cell Biology Lab), School of Sciences, Gujarat University, Ahmedabad.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't