Your search returned 143 results.

Results
	1.	Cohesin embraces new phenotypes. [electronic resource] by Krantz, Ian D Producer: 20150120 In: Nature genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Alagille syndrome: chipping away at the tip of the iceberg. [electronic resource] by Krantz, Ian D Producer: 20030311 In: American journal of medical genetics vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	On the molecular etiology of Cornelia de Lange syndrome. [electronic resource] by Dorsett, Dale Krantz, Ian D Producer: 20090210 In: Annals of the New York Academy of Sciences vol. 1151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Cohesin biology and the cohesinopathies: Abstracts from the Second Biennial Conference, Pontignano, Italy, 2009. [electronic resource] by Musio, Antonio Krantz, Ian D Producer: 20100929 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Cohesin and human disease. [electronic resource] by Liu, Jinglan Krantz, Ian D Producer: 20081204 In: Annual review of genomics and human genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Pallister-Killian syndrome. [electronic resource] by Izumi, Kosuke Krantz, Ian D Producer: 20150818 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 166C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Introduction--a Pallister jubilee. [electronic resource] by Krantz, Ian D Opitz, John M Producer: 20150818 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 166C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Expanded non-invasive prenatal diagnostics. [electronic resource] by Spinner, Nancy B Krantz, Ian D Producer: 20190430 In: Nature medicine vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Novel microdeletion syndromes. [electronic resource] by Krantz, Ian D Spinner, Nancy B Producer: 20080117 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 145C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome. [electronic resource] by Izumi, Kosuke Zhang, Zhe Kaur, Maninder Krantz, Ian D Producer: 20150729 In: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Interstitial deletion of 7q22.1q31.1 in a boy with structural brain abnormality, cardiac defect, developmental delay, and dysmorphic features. [electronic resource] by Katz, Olivia L Krantz, Ian D Noon, Sarah E Producer: 20171003 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Characterization of DNA methylation and its association with other biological systems in lymphoblastoid cell lines. [electronic resource] by Zhang, Zhe Liu, Jinglan Kaur, Maninder Krantz, Ian D Producer: 20120723 In: Genomics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	NKX2.5 mutation identification on exome sequencing in a patient with heterotaxy. [electronic resource] by Izumi, Kosuke Noon, Sarah Wilkens, Alisha Krantz, Ian D Producer: 20150612 In: European journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion. [electronic resource] by Ramos, Maria Wilkens, Alisha Krantz, Ian D Wu, Yaning Producer: 20171003 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Spectrum and consequences of SMC1A mutations: the unexpected involvement of a core component of cohesin in human disease. [electronic resource] by Mannini, Linda Liu, Jinglan Krantz, Ian D Musio, Antonio Producer: 20100312 In: Human mutation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Dr. Laird G. Jackson Festschrift. [electronic resource] by Noon, Sarah E Deardorff, Matthew A Krantz, Ian D Producer: 20180126 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Cardiac manifestations of Pallister-Killian syndrome. [electronic resource] by Tilton, Richard K Wilkens, Alisha Krantz, Ian D Izumi, Kosuke Producer: 20150820 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)
	18.	A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss. [electronic resource] by Zhao, Jianhua Noon, Sarah E Krantz, Ian D Wu, Yaning Producer: 20171003 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mutation spectrum and genotype-phenotype correlation in Cornelia de Lange syndrome. [electronic resource] by Mannini, Linda Cucco, Francesco Quarantotti, Valentina Krantz, Ian D Musio, Antonio Producer: 20140616 In: Human mutation vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	NIPBL Controls RNA Biogenesis to Prevent Activation of the Stress Kinase PKR. [electronic resource] by Yuen, Kobe C Xu, Baoshan Krantz, Ian D Gerton, Jennifer L Producer: 20160929 In: Cell reports vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

1
2
3
4
5
6
7
8
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 143 results.