Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity

By Banatao D.R.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1229-1234

Oxford University Press

Access to resources Recommend Favorite

Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH

By  

Molecular Syndromology, Vol. 2, Iss. 2, 2012-01 ,pp. : 88-93

Karger

Access to resources Recommend Favorite

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics

By Qiao Y.   Harvard C.   Tyson C.   Liu X.   Fawcett C.   Pavlidis P.   Holden J.   Lewis M.   Rajcan-Separovic E.  

Human Genetics, Vol. 128, Iss. 2, 2010-08 ,pp. : 179-194

Springer Publishing Company

Access to resources Recommend Favorite

Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: An array‐CGH study

By  

American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2597-2600

John Wiley & Sons Inc

Access to resources Recommend Favorite

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

By de Smith Adam J.   Tsalenko Anya   Sampas Nick   Scheffer Alicia   Yamada N. Alice   Tsang Peter   Ben-Dor Amir   Yakhini Zohar   Ellis Richard J.   Bruhn Laurakay   Laderman Stephen   Froguel Philippe   Blakemore Alexandra I.F.  

Human Molecular Genetics, Vol. 16, Iss. 23, 2007-12 ,pp. : 2783-2794

Oxford University Press

Access to resources Recommend Favorite