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	1.	The origin of four squirrel monkey cell lines established by karyotype analysis. [electronic resource] by Scammell, J G Wright, J L Tuck-Muller, C M Producer: 20011004 In: Cytogenetics and cell genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Autosomal dominant congenital cataract associated with chromosomal translocation [t(3;4)(p26.2;p15)]. [electronic resource] by Reese, P D Tuck-Muller, C M Maumenee, I H Producer: 19871110 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene. [electronic resource] by Youssoufian, H Chance, P Tuck-Muller, C M Jabs, E W Producer: 19880418 In: Human genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Fertility and the cri du chat syndrome. [electronic resource] by Martínez, J E Tuck-Muller, C M Superneau, D Wertelecki, W Producer: 19930816 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization. [electronic resource] by Chen, H Tuck-Muller, C M Batista, D A Wertelecki, W Producer: 19950828 In: American journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Hyperlipidemia, insulin-dependent diabetes mellitus, and rapidly progressive diabetic retinopathy and nephropathy in Prader-Willi syndrome with del(15)(q11.2q13). [electronic resource] by Bassali, R Hoffman, W H Chen, H Tuck-Muller, C M Producer: 19971114 In: American journal of medical genetics vol. 71 Availability: No items available. Save to lists Add to cart (remove)
	7.	NOR associations with heterochromatin. [electronic resource] by Tuck-Muller, C M Bordson, B L Varela, M Bennett, J W Producer: 19841128 In: Cytogenetics and cell genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Studies of mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism. [electronic resource] by Jabs, E W Tuck-Muller, C M Cusano, R Rattner, J B Producer: 19910801 In: Chromosoma vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A rapid method for PCR amplification of DNA directly from cells fixed in Carnoy's fixative. [electronic resource] by Li, S Tuck-Muller, C M Yan, Q Wertelecki, W Chen, H Producer: 19950504 In: American journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Centromere separation and aneuploidy in human mitotic mutants: Roberts syndrome. [electronic resource] by Jabs, E W Tuck-Muller, C M Cusano, R Rattner, J B Producer: 19900412 In: Progress in clinical and biological research vol. 318 Availability: No items available. Save to lists Add to cart (remove)
	11.	Correction of sphingomyelinase deficiency in Niemann-Pick type C fibroblasts by removal of lipoprotein fraction from culture media. [electronic resource] by Thomas, G H Tuck-Muller, C M Miller, C S Reynolds, L W Producer: 19890901 In: Journal of inherited metabolic disease vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Cancer susceptibility in ataxia-telangiectasia. [electronic resource] by Peterson, R D Funkhouser, J D Tuck-Muller, C M Gatti, R A Producer: 19920423 In: Leukemia vol. 6 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	13.	A method for combined C-banding and silver staining. [electronic resource] by Tuck-Muller, C M Bordson, B L Kane, M M Hamilton, A E Producer: 19850118 In: Stain technology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	1p microdeletion in sibs with minimal phenotypic manifestations. [electronic resource] by Martínez, J E Tuck-Muller, C M Gasparrini, W Li, S Wertelecki, W Producer: 19990329 In: American journal of medical genetics vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	15.	Chromosome studies in 10 patients with the Rett syndrome. [electronic resource] by Moore, J W Tuck-Muller, C M Murphy, M Naidu, S Thomas, G H Producer: 19860627 In: American journal of medical genetics. Supplement vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample. [electronic resource] by Ehrlich, M Tsien, F Herrera, D Blackman, V Roggenbuck, J Tuck-Muller, C M Producer: 20020307 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Adrenal insufficiency in Smith-Lemli-Opitz syndrome. [electronic resource] by Andersson, H C Frentz, J Martínez, J E Tuck-Muller, C M Bellizaire, J Producer: 19990517 In: American journal of medical genetics vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	18.	A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspring. [electronic resource] by Tuck-Muller, C M Varela, M Li, S Pridjian, G Chen, H Wertelecki, W Producer: 19961107 In: American journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Duplication of the short arm of the X chromosome in mother and daughter. [electronic resource] by Tuck-Muller, C M Martinez, J E Batista, D A Kearns, W G Wertelecki, W Producer: 19930701 In: Human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Translocation 10;18 in a patient with juvenile neuronal ceroid-lipofuscinosis (Batten disease). [electronic resource] by Tuck-Muller, C M Dyken, P R Li, S Chen, H Labbé, E Wertelecki, W Producer: 19951011 In: American journal of medical genetics vol. 57 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 34 results.