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Archives of Disease in Childhood
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November 23, 2005
Chromosome analysis: what and when to request
F H Sharkey, E Maher, D R FitzPatrick
Molecular Syndromology
|
November 4, 2010
Interstitial Deletions at 6q14.1-q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype
C Wentzel, S A Lynch, E-L Stattin, et al.
Cytogenetic and Genome Research
|
January 30, 2010
17q21.31 microdeletion syndrome: further expanding the clinical phenotype
F H Sharkey, N Morrison, R Murray, et al.
Cytogenetic and Genome Research
|
March 17, 2009
Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting
S Goobie, J Knijnenburg, D Fitzpatrick, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Archives of Disease in Childhood
|
November 23, 2005
Chromosome analysis: what and when to request
F H Sharkey, E Maher, D R FitzPatrick
Molecular Syndromology
|
November 4, 2010
Interstitial Deletions at 6q14.1-q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype
C Wentzel, S A Lynch, E-L Stattin, et al.
Cytogenetic and Genome Research
|
January 30, 2010
17q21.31 microdeletion syndrome: further expanding the clinical phenotype
F H Sharkey, N Morrison, R Murray, et al.
Cytogenetic and Genome Research
|
March 17, 2009
Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting
S Goobie, J Knijnenburg, D Fitzpatrick, et al.
Page
of 1