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	1.	Silver-Russell syndrome: genetic basis and molecular genetic testing. [electronic resource] by Eggermann, Thomas Begemann, Matthias Binder, Gerhard Spengler, Sabrina Producer: 20101101 In: Orphanet journal of rare diseases vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations. [electronic resource] by Eggermann, Thomas Begemann, Matthias Kurth, Ingo Elbracht, Miriam Producer: 20190904 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Testing of buccal swab DNA does not increase the detection rate for imprinting control region 1 hypomethylation in Silver-Russell syndrome. [electronic resource] by Spengler, Sabrina Begemann, Matthias Binder, Gerhard Eggermann, Thomas Producer: 20120203 In: Genetic testing and molecular biomarkers vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Silver-Russell syndrome. [electronic resource] by Binder, Gerhard Begemann, Matthias Eggermann, Thomas Kannenberg, Kai Producer: 20110705 In: Best practice & research. Clinical endocrinology & metabolism vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Epigenetic and genetic diagnosis of Silver-Russell syndrome. [electronic resource] by Eggermann, Thomas Spengler, Sabrina Gogiel, Magdalena Begemann, Matthias Elbracht, Miriam Producer: 20121218 In: Expert review of molecular diagnostics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders. [electronic resource] by Müller, Anne Soellner, Lukas Binder, Gerhard Begemann, Matthias Eggermann, Thomas Producer: 20161019 In: American journal of medical genetics. Part A vol. 170A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders. [electronic resource] by Eggermann, Thomas Leisten, Isabelle Binder, Gerhard Begemann, Matthias Spengler, Sabrina Producer: 20120423 In: Epigenomics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylation. [electronic resource] by Begemann, Matthias Spengler, Sabrina Kordass, Ulrike Schröder, Carmen Eggermann, Thomas Producer: 20120720 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Next generation sequencing and imprinting disorders: Current applications and future perspectives: Lessons from Silver-Russell syndrome. [electronic resource] by Neuheuser, Lea Meyer, Robert Begemann, Matthias Elbracht, Miriam Eggermann, Thomas Producer: 20190506 In: Molecular and cellular probes vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequences. [electronic resource] by Elbracht, Miriam Mackay, Deborah Begemann, Matthias Kagan, Karl Oliver Eggermann, Thomas Producer: 20201201 In: Human reproduction update vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Genetic and epigenetic findings in Silver-Russell syndrome. [electronic resource] by Eggermann, Thomas Begemann, Matthias Spengler, Sabrina Schröder, Carmen Kordass, Ulrike Binder, Gerhard Producer: 20110125 In: Pediatric endocrinology reviews : PER vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	12.	First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylation. [electronic resource] by Riess, Angelika Binder, Gerhard Ziegler, Julian Begemann, Matthias Soellner, Lukas Eggermann, Thomas Producer: 20161018 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)
	13.	Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation. [electronic resource] by Kraft, Florian Wesseler, Katharina Begemann, Matthias Kurth, Ingo Elbracht, Miriam Eggermann, Thomas Producer: 20190820 In: Clinical epigenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients. [electronic resource] by Eggermann, Thomas Ledig, Susanne Begemann, Matthias Elbracht, Miriam Kurth, Ingo Wieacker, Peter Producer: 20190123 In: Molecular genetics & genomic medicine vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci. [electronic resource] by Begemann, Matthias Leisten, Isabelle Soellner, Lukas Zerres, Klaus Eggermann, Thomas Spengler, Sabrina Producer: 20121011 In: Epigenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring. [electronic resource] by Soellner, Lukas Begemann, Matthias Degenhardt, Franziska Geipel, Annegret Eggermann, Thomas Mangold, Elisabeth Producer: 20171212 In: European journal of human genetics : EJHG vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Congenital imprinting disorders: Application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management. [electronic resource] by Soellner, Lukas Monk, David Rezwan, Faisal I Begemann, Matthias Mackay, Deborah Eggermann, Thomas Producer: 20160923 In: Molecular and cellular probes vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	IGF1R mutation analysis in short children with Silver-Russell syndrome features. [electronic resource] by Soellner, Lukas Spengler, Sabrina Begemann, Matthias Wollmann, Hartmut A Binder, Gerhard Eggermann, Thomas Producer: 20160914 In: Journal of pediatric genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. [electronic resource] by Soellner, Lukas Kraft, Florian Sauer, Sabrina Begemann, Matthias Kurth, Ingo Elbracht, Miriam Eggermann, Thomas Producer: 20190411 In: European journal of human genetics : EJHG vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Identification of transcription factor binding sites using ATAC-seq. [electronic resource] by Li, Zhijian Schulz, Marcel H Look, Thomas Begemann, Matthias Zenke, Martin Costa, Ivan G Producer: 20190321 In: Genome biology vol. 20 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 48 results.