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	921.	Assignment of human KH-box-containing genes by in situ hybridization: HNRNPK maps to 9q21.32-q21.33, PCBP1 to 2p12-p13, and PCBP2 to 12q13.12-q13.13, distal to FRA12A. [electronic resource] by Tommerup, N Leffers, H Producer: 19970529 In: Genomics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	922.	Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly. [electronic resource] by Roessler, E Ward, D E Gaudenz, K Belloni, E Scherer, S W Donnai, D Siegel-Bartelt, J Tsui, L C Muenke, M Producer: 19970908 In: Human genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	923.	Dominant inheritance of cleft palate, microstomia and micrognathia--possible linkage to the fragile site at 16q22 (FRA16B). [electronic resource] by McKenzie, F Turner, A Withers, S Dalzell, P McGlynn, M Kirk, E P E Producer: 20030312 In: Clinical dysmorphology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	924.	Chromosomal aberrations, sister chromatid exchanges and high frequency cells in young patients with neurofibromatosis 1 (NF1). [electronic resource] by Bigatti, M P Ardito, G Lamberti, L Crovella, S Collell, M Giordanino, S Benso, L Producer: 20001026 In: Neoplasma vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	925.	A common region of allelic loss on chromosome region 3p25.3-26.3 in nasopharyngeal carcinoma. [electronic resource] by Deng, L Jing, N Tan, G Zhou, M Zhan, F Xie, Y Cao, L Li, G Producer: 19980930 In: Genes, chromosomes & cancer vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	926.	In vitro effect of fludarabine, cyclophosphamide, and cytosine arabinoside on chromosome breakage in Fanconi anemia patients: relevance to stem cell transplantation. [electronic resource] by Yabe, Miharu Yabe, Hiromasa Hamanoue, Satoshi Inoue, Hiroyasu Matsumoto, Masae Koike, Takashi Ishiguro, Hiroyuki Morimoto, Tsuyoshi Arakawa, Satoshi Ohshima, Toshio Masukawa, Atsuko Miyachi, Hayato Yamashita, Takayuki Katob, Shunichi Producer: 20070806 In: International journal of hematology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	927.	Establishing nucleosome architecture and stability at promoters: Roles of pioneer transcription factors and the RSC chromatin remodeler. [electronic resource] by Kubik, Slawomir Bruzzone, Maria Jessica Shore, David Producer: 20180205 In: BioEssays : news and reviews in molecular, cellular and developmental biology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	928.	Breakpoint localization within the M-bcr and clinical course do not correlate in patients with chronic myelogenous leukemia undergoing alfa interferon therapy. [electronic resource] by Opalka, B Wandl, U Beer, U Roggenbuck, U Kloke, O Niederle, N Producer: 19910726 In: Leukemia vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	929.	Penetrance and low concordance in monozygotic twins in disease: are they the results of alterations in somatic genomes? [electronic resource] by Kastern, W Kryspin-Sorensen, I Producer: 19900410 In: Molecular reproduction and development vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	930.	A tissue-specific fragile site associated with the sex reversed (Sxr) mutation in the mouse. [electronic resource] by Hunt, P A Burgoyne, P S Producer: 19880407 In: Chromosoma vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	931.	Experience with prenatal fragile X detection. [electronic resource] by Jenkins, E C Brown, W T Brooks, J Duncan, C J Rudelli, R D Wisniewski, H M Producer: 19840511 In: American journal of medical genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	932.	Hypomethylation of chromosome 1 heterochromatin DNA correlates with q-arm copy gain in human hepatocellular carcinoma. [electronic resource] by Wong, N Lam, W C Lai, P B Pang, E Lau, W Y Johnson, P J Producer: 20010906 In: The American journal of pathology vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	933.	The female and the fragile X reviewed. [electronic resource] by Kenneson, A Warren, S T Producer: 20011231 In: Seminars in reproductive medicine vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	934.	Chromosomal fragility in a behavioral disorder. [electronic resource] by Arrieta, Isabel Núñez, Teresa Martínez, Begoña Pérez, Arantza Télez, Mercedes Criado, Begoña Gainza, Itziar Lostao, Carlos M Producer: 20030219 In: Behavior genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	935.	Equal induction and persistence of chromosome aberrations involving chromosomes with heterogeneous lengths and gene densities. [electronic resource] by Puerto, S Surrallés, J Ramírez, M J Creus, A Marcos, R Producer: 20000516 In: Cytogenetics and cell genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	936.	The expression of folate sensitive fragile sites in patients with bipolar disorder. [electronic resource] by Demirhan, Osman Tastemir, Deniz Sertdemir, Yasar Producer: 20090511 In: Yonsei medical journal vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	937.	Distribution of X-ray-induced chromosome breakpoints in Down syndrome lymphocytes. [electronic resource] by Shafik, H M Au, W W Whorton, E B Legator, M S Producer: 19910416 In: American journal of medical genetics. Supplement vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	938.	The expression frequency of common fragile sites and genetic susceptibility to lung cancers. [electronic resource] by Liu, C X Wang, G H Li, P Producer: 19891101 In: Cancer genetics and cytogenetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	939.	A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerations. [electronic resource] by Shabtai, F Klar, D Nissimov, R Vardimon, D Hart, J Halbrecht, I Producer: 19831028 In: Human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	940.	[Metabolism of monocarbons and the fragile X syndrome]. [electronic resource] by Lejeune, J Producer: 19820826 In: Bulletin de l'Academie nationale de medecine vol. 165 Availability: No items available. Save to lists Add to cart (remove)

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