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	1.	Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation. [electronic resource] by Ahlbom, B E Sidenvall, R Annerén, G Producer: 19961227 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus. [electronic resource] by Ahlbom, B E Dahl, N Zetterqvist, P Annerén, G Producer: 19951214 In: Clinical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Linkage analysis excludes familial congenital hypothyroidism from chromosome 21. [electronic resource] by Ahlbom, B E Yaqoob, M Annerén, G Larsson, A Ilicki, A Wadelius, C Producer: 19990414 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	4.	Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype. [electronic resource] by Ahlbom, B E Goetz, P Korenberg, J R Pettersson, U Seemanova, E Wadelius, C Zech, L Annerén, G Producer: 19970320 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)

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