Your search returned 28 results.

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	1.	Laboratory aspects of prenatal microarray analysis. [electronic resource] by Lamb, Allen N Producer: 20120531 In: Clinics in laboratory medicine vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advances. [electronic resource] by South, Sarah T Lamb, Allen N Producer: 20130318 In: Expert opinion on medical diagnostics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cytogenetics and molecular cytogenetics in prenatal diagnosis. [electronic resource] by Donnenfeld, Alan E Lamb, Allen N Producer: 20040106 In: Clinics in laboratory medicine vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literature. [electronic resource] by Herriges, John C Dugan, Sarah L Lamb, Allen N Publication details: Molecular cytogenetics 2019 In: Molecular cytogenetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Prenatal diagnosis from fetal urine in bladder outlet obstruction: success rates for traditional cytogenetic evaluation and interphase fluorescence in situ hybridization. [electronic resource] by Donnenfeld, Alan E Lockwood, David Custer, Trace Lamb, Allen N Producer: 20030507 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder. [electronic resource] by Bhat, Gifty LaGrave, Danielle Millson, Alison Herriges, John Lamb, Allen N Matalon, Reuben Producer: 20170202 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability. [electronic resource] by Andersen, Erica F Baldwin, Erin E Ellingwood, Sara Smith, Rosemarie Lamb, Allen N Producer: 20150818 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013. [electronic resource] by South, Sarah T Lee, Charles Lamb, Allen N Higgins, Anne W Kearney, Hutton M Producer: 20140616 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray. [electronic resource] by Coppinger, Justine Alliman, Sarah Lamb, Allen N Torchia, Beth S Bejjani, Bassem A Shaffer, Lisa G Producer: 20100205 In: Prenatal diagnosis vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay. [electronic resource] by Paulraj, Prabakaran Bosworth, Michelle Longhurst, Maria Hornbuckle, Callie Gotway, Garrett Lamb, Allen N Andersen, Erica F Producer: 20191203 In: Cytogenetic and genome research vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature. [electronic resource] by Herriges, John C Arch, Ellen M Burgio, Pamela A Baldwin, Erin E LaGrave, Danielle Lamb, Allen N Toydemir, Reha M Producer: 20200324 In: Journal of child neurology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis. [electronic resource] by Lamb, Allen N Rosenfeld, Jill A Coppinger, Justine Dodge, Erin T Dabell, Mindy Preston Torchia, Beth S Ravnan, J Britt Shaffer, Lisa G Ballif, Blake C Producer: 20130408 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH. [electronic resource] by Neill, Nicholas J Ballif, Blake C Lamb, Allen N Parikh, Sumit Ravnan, J Britt Schultz, Roger A Torchia, Beth S Rosenfeld, Jill A Shaffer, Lisa G Producer: 20110713 In: Genome research vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate. [electronic resource] by Sahoo, Trilochan Theisen, Aaron Sanchez-Lara, Pedro A Marble, Michael Schweitzer, Daniela N Torchia, Beth S Lamb, Allen N Bejjani, Bassem A Shaffer, Lisa G Lacassie, Yves Producer: 20111014 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. [electronic resource] by Sahoo, Trilochan Theisen, Aaron Rosenfeld, Jill A Lamb, Allen N Ravnan, J Britt Schultz, Roger A Torchia, Beth S Neill, Nicholas Casci, Ian Bejjani, Bassem A Shaffer, Lisa G Producer: 20120208 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). [electronic resource] by Waggoner, Darrel Wain, Karen E Dubuc, Adrian M Conlin, Laura Hickey, Scott E Lamb, Allen N Martin, Christa Lese Morton, Cynthia C Rasmussen, Kristen Schuette, Jane L Schwartz, Stuart Miller, David T Producer: 20190226 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome. [electronic resource] by Duker, Angela L Ballif, Blake C Bawle, Erawati V Person, Richard E Mahadevan, Sangeetha Alliman, Sarah Thompson, Regina Traylor, Ryan Bejjani, Bassem A Shaffer, Lisa G Rosenfeld, Jill A Lamb, Allen N Sahoo, Trilochan Producer: 20110302 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Clinical features associated with copy number variations of the 14q32 imprinted gene cluster. [electronic resource] by Rosenfeld, Jill A Fox, Joyce E Descartes, Maria Brewer, Fallon Stroud, Tracy Gorski, Jerome L Upton, Sheila J Moeschler, John B Monteleone, Berrin Neill, Nicholas J Lamb, Allen N Ballif, Blake C Shaffer, Lisa G Ravnan, J Britt Producer: 20150916 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes. [electronic resource] by Rosenfeld, Jill A Drautz, Joanne Milisa Clericuzio, Carol L Cushing, Tom Raskin, Salmo Martin, Judith Tervo, Raymond C Pitarque, Jose A Nowak, Dorota M Karolak, Justyna A Lamb, Allen N Schultz, Roger A Ballif, Blake C Bejjani, Bassem A Gajecka, Marzena Shaffer, Lisa G Producer: 20111123 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes. [electronic resource] by Shaffer, Lisa G Coppinger, Justine Morton, S Annie Alliman, Sarah Burleson, Jessica Traylor, Ryan Walker, Cathryn Byerly, Steve Lamb, Allen N Schultz, Roger Ravnan, J Britt Kashork, Catherine D Torchia, Beth S Sulpizio, Scott Sundin, Kyle Schermer, Mack Adler, Karl Dallaire, Stephanie Ballif, Blake C Producer: 20111201 In: Prenatal diagnosis vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 28 results.