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	1.	Protocolized management of infants with congenital diaphragmatic hernia: effect on survival. [electronic resource] by Antonoff, Mara B Hustead, Virginia A Groth, Shawn S Schmeling, David J Producer: 20110627 In: Journal of pediatric surgery vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Spontaneous tracheal and subglottic tears in neonates. [electronic resource] by Kacmarynski, Deborah S F Sidman, James D Rimell, Frank L Hustead, Virginia A Producer: 20020927 In: The Laryngoscope vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Craniosynostosis: another feature of the 22q11.2 deletion syndrome. [electronic resource] by McDonald-McGinn, Donna M Gripp, Karen W Kirschner, Richard E Maisenbacher, Melissa K Hustead, Virginia Schauer, Galen M Keppler-Noreuil, Kim M Ciprero, Karen L Pasquariello, Patrick LaRossa, Don Bartlett, Scott P Whitaker, Linton A Zackai, Elaine H Producer: 20050822 In: American journal of medical genetics. Part A vol. 136A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder. [electronic resource] by Szafranski, Przemyslaw Dharmadhikari, Avinash V Brosens, Erwin Gurha, Priyatansh Kolodziejska, Katarzyna E Zhishuo, Ou Dittwald, Piotr Majewski, Tadeusz Mohan, K Naga Chen, Bo Person, Richard E Tibboel, Dick de Klein, Annelies Pinner, Jason Chopra, Maya Malcolm, Girvan Peters, Gregory Arbuckle, Susan Guiang, Sixto F Hustead, Virginia A Jessurun, Jose Hirsch, Russel Witte, David P Maystadt, Isabelle Sebire, Neil Fisher, Richard Langston, Claire Sen, Partha Stankiewicz, Paweł Producer: 20130611 In: Genome research vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations. [electronic resource] by Stankiewicz, Paweł Sen, Partha Bhatt, Samarth S Storer, Mekayla Xia, Zhilian Bejjani, Bassem A Ou, Zhishuo Wiszniewska, Joanna Driscoll, Daniel J Maisenbacher, Melissa K Bolivar, Juan Bauer, Mislen Zackai, Elaine H McDonald-McGinn, Donna Nowaczyk, Małgorzata M J Murray, Mitzi Hustead, Virginia Mascotti, Kristin Schultz, Regina Hallam, Lavinia McRae, Duncan Nicholson, Andrew G Newbury, Robert Durham-O'Donnell, Jane Knight, Gail Kini, Usha Shaikh, Tamim H Martin, Vicki Tyreman, Matthew Simonic, Ingrid Willatt, Lionel Paterson, Joan Mehta, Sarju Rajan, Diana Fitzgerald, Tomas Gribble, Susan Prigmore, Elena Patel, Ankita Shaffer, Lisa G Carter, Nigel P Cheung, Sau Wai Langston, Claire Shaw-Smith, Charles Producer: 20090702 In: American journal of human genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)