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	1.	Diminished capping of lymphocytes from pregnant women. [electronic resource] by Kosower, N S Shomrat, R Producer: 19840107 In: American journal of reproductive immunology : AJRI : official journal of the American Society for the Immunology of Reproduction and the International Coordination Committee for Immunology of Reproduction vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APC mutation in exon 9. [electronic resource] by Rozen, P Samuel, Z Shomrat, R Legum, C Producer: 20000119 In: Gut vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy. [electronic resource] by Shomrat, R Driks, N Legum, C Shiloh, Y Producer: 19920323 In: American journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients. [electronic resource] by Legum, C Shomrat, R Glassner, M Shiloh, Y Producer: 19950322 In: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Muir-Torre syndrome and HNPCC: importance of clinical diagnosis and genetic investigation in family members]. [electronic resource] by Strul, H Rozen, P Naiman, T Shomrat, R Producer: 20000915 In: Harefuah vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	6.	Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients. [electronic resource] by Shomrat, R Gluck, E Legum, C Shiloh, Y Producer: 19940517 In: American journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene. [electronic resource] by Shalitin, S Josefsberg, Z Vilain, E Shomrat, R Weintrob, N Producer: 20030130 In: Molecular genetics and metabolism vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Early pregnancy screening for neural tube defects in Israel. [electronic resource] by Legum, C Shomrat, R Yedwab, G Jaffa, A J Rudick, A Producer: 19860930 In: Israel journal of medical sciences vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	9.	Dynamic changes of red cell membrane thiol groups followed by bimane fluorescent labeling. [electronic resource] by Kosower, N S Kosower, E M Zipser, Y Faltin, Z Shomrat, R Producer: 19810613 In: Biochimica et biophysica acta vol. 640 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family. [electronic resource] by Frydman, M Straussberg, R Shomrat, R Goebel, H Legum, C Shiloh, Y Producer: 19960130 In: American journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy. [electronic resource] by Nevo, Y Shomrat, R Yaron, Y Orr-Urtreger, A Harel, S Legum, C Producer: 19991208 In: Prenatal diagnosis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	[Familial adenomatous polyposis: establishing a registry and genetic and molecular analysis]. [electronic resource] by Shomrat, R Bruchim, R Galanty, Y Samuel, Z Legum, C Rabau, M Rozen, P Producer: 19970421 In: Harefuah vol. 132 Availability: No items available. Save to lists Add to cart (remove)
	13.	High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish origin. [electronic resource] by Shahrabani-Gargir, L Shomrat, R Yaron, Y Orr-Urtreger, A Groden, J Legum, C Producer: 19991012 In: Genetic testing vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Detection of Duchenne muscular dystrophy gene products in amniotic fluid and chorionic villus sampling cells. [electronic resource] by Prigojin, H Brusel, M Fuchs, O Shomrat, R Legum, C Nudel, U Yaffe, D Producer: 19940107 In: FEBS letters vol. 335 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer. [electronic resource] by Rozen, P Shomrat, R Strul, H Naiman, T Karminsky, N Legum, C Orr-Urtreger, A Producer: 19990126 In: Gastroenterology vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Familial adenomatous polyposis at the Tel Aviv Medical Center: demographic and clinical features. [electronic resource] by Rozen, P Samuel, Z Rabau, M Goldman, G Shomrat, R Legum, C Orr-Urtreger, A Producer: 20031216 In: Familial cancer vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Novel mutations in the emerin gene in Israeli families. [electronic resource] by Nevo, Y Ahituv, S Yaron, Y Kedmi, M Shomrat, R Legum, C Orr-Urtreger, A Producer: 20011025 In: Human mutation vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Ultrastructure of the conjunctiva, skin, and gingiva: a case of Sandhoff's disease in a Jewish patient. [electronic resource] by Messer, G Harel, S Erlich, B Navon, R Nemet, P Sarnat, H Shomrat, R Legum, C Producer: 19800426 In: Archives of pathology & laboratory medicine vol. 104 Availability: No items available. Save to lists Add to cart (remove)
	19.	SMA type 2 unrelated to chromosome 5q13. [electronic resource] by Nevo, Y Kramer, U Legum, C Shomrat, R Fatal, A Soffer, D Harel, S Shapira, Y Producer: 19980324 In: American journal of medical genetics vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	20.	The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families. [electronic resource] by Geva, E Yaron, Y Shomrat, R Ben-Yehuda, A Zabari, S Peretz, H Naiman, T Yeger, H Orr-Urtreger, A Producer: 20010201 In: Genetic testing vol. 4 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 22 results.