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1.
Interstitial deletion of 1p22.2p31.1 and medium-chain acyl-CoA dehydrogenase deficiency in a patient with global developmental delay.
Am J Med Genet A
; 146A(12): 1581-6, 2008 Jun 15.
Article
in English
| MEDLINE | ID: mdl-18478588
2.
Detecting rearrangements in children using subtelomeric FISH and SKY.
Am J Med Genet
; 107(4): 267-74, 2002 Feb 01.
Article
in English
| MEDLINE | ID: mdl-11840482
3.
Array-based genomic delineation of a familial duplication 11q14.1-q22.1 associated with recurrent depression.
Am J Med Genet B Neuropsychiatr Genet
; 141B(3): 214-9, 2006 Apr 05.
Article
in English
| MEDLINE | ID: mdl-16526031
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