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	1.	Concerns regarding transience and heterozygosity in neonatal hyperglycenemia. [electronic resource] by Hamosh, Ada Van Hove, Johan Producer: 20030604 In: Annals of neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes. [electronic resource] by Amberger, Joanna S Hamosh, Ada Producer: 20171106 In: Current protocols in bioinformatics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Genomic Data Sharing for Novel Mendelian Disease Gene Discovery: The Matchmaker Exchange. [electronic resource] by Azzariti, Danielle R Hamosh, Ada Producer: 20210624 In: Annual review of genomics and human genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®). [electronic resource] by Amberger, Joanna Bocchini, Carol Hamosh, Ada Producer: 20111012 In: Human mutation vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	GeneMatcher: a matching tool for connecting investigators with an interest in the same gene. [electronic resource] by Sobreira, Nara Schiettecatte, François Valle, David Hamosh, Ada Producer: 20160629 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	New tools for Mendelian disease gene identification: PhenoDB variant analysis module; and GeneMatcher, a web-based tool for linking investigators with an interest in the same gene. [electronic resource] by Sobreira, Nara Schiettecatte, François Boehm, Corinne Valle, David Hamosh, Ada Producer: 20151217 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Horizontal integration of OMIM across the medical school preclinical curriculum for early reinforcement of clinical genetics principles. [electronic resource] by Diehl, Adam C Reader, Lauren Hamosh, Ada Bodurtha, Joann N Producer: 20150918 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	McKusick's Online Mendelian Inheritance in Man (OMIM). [electronic resource] by Amberger, Joanna Bocchini, Carol A Scott, Alan F Hamosh, Ada Producer: 20090303 In: Nucleic acids research vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). [electronic resource] by Ferreira, Carlos Poretti, Andrea Cohen, Julie Hamosh, Ada Naidu, Sakkubai 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)
	10.	Bioinformatics for medical students: a 5-year experience using OMIM® in medical student education. [electronic resource] by Lee-Barber, Jasmine Kulo, Violet Lehmann, Harold Hamosh, Ada Bodurtha, Joann Producer: 20191112 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	False negative cystic fibrosis newborn screen. [electronic resource] by Collaco, Joseph Michael Panny, Susan R Hamosh, Ada Mogayzel, Peter J Producer: 20100519 In: Clinical pediatrics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	OMIM.org: leveraging knowledge across phenotype-gene relationships. [electronic resource] by Amberger, Joanna S Bocchini, Carol A Scott, Alan F Hamosh, Ada Producer: 20200518 In: Nucleic acids research vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Maternal hyperphenylalaninemia: rapid achievement of metabolic control predicts overall control throughout pregnancy. [electronic resource] by Martino, Teresa Koerner, Celide Yenokyan, Gayane Hoover-Fong, Julie Hamosh, Ada Producer: 20131112 In: Molecular genetics and metabolism vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders. [electronic resource] by Amberger, Joanna S Bocchini, Carol A Schiettecatte, François Scott, Alan F Hamosh, Ada Producer: 20150629 In: Nucleic acids research vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Problematic variation in local institutional review of a multicenter genetic epidemiology study. [electronic resource] by McWilliams, Rita Hoover-Fong, Julie Hamosh, Ada Beck, Suzanne Beaty, Terri Cutting, Garry Producer: 20030718 In: JAMA vol. 290 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. [electronic resource] by Hamosh, Ada Scott, Alan F Amberger, Joanna Bocchini, Carol Valle, David McKusick, Victor A Producer: 20020121 In: Nucleic acids research vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. [electronic resource] by Hamosh, Ada Scott, Alan F Amberger, Joanna S Bocchini, Carol A McKusick, Victor A Producer: 20050415 In: Nucleic acids research vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition. [electronic resource] by Li, Feng Lisi, Emily C Wohler, Elizabeth S Hamosh, Ada Batista, Denise A S Producer: 20091113 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization. [electronic resource] by Cain, Colyn Cargile Saul, Daniel Attanasio, Lisa Oehler, Erin Hamosh, Ada Blakemore, Karin Stetten, Gail Producer: 20070605 In: Prenatal diagnosis vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	A novel presentation of DYT 16: acute onset in infancy and association with MRI abnormalities. [electronic resource] by Lemmon, Monica E Lavenstein, Bennett Applegate, Carolyn D Hamosh, Ada Tekes, Aylin Singer, Harvey S Producer: 20140729 In: Movement disorders : official journal of the Movement Disorder Society vol. 28 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 65 results.