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	81.	Establishment and characterization of a new human urinary bladder carcinoma cell line (PS-1). [electronic resource] by Sanford, E J Geder, L Dagen, J E Laychock, A M Ladda, R Rohner, T J Producer: 19790115 In: Investigative urology vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	82.	Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations. [electronic resource] by Ramer, J C Mowrey, P N Robins, D B Ligato, S Towfighi, J Ladda, R L Producer: 19910131 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant Coloboma. [electronic resource] by Hess, E J Rogan, P K Domoto, M Tinker, D E Ladda, R L Ramer, J C Producer: 19961205 In: American journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation. [electronic resource] by Ramer, J C Lin, A E Dobyns, W B Winter, R Aymé, S Pallotta, R Ladda, R L Producer: 19951019 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)
	85.	Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindred. [electronic resource] by Dow, E Cross, S Wolgemuth, D J Lyonnet, S Mulligan, L M Mascari, M Ladda, R Williamson, R Producer: 19950126 In: American journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Effect of differentiation inducers on growth characteristics of human glioma cell lines. [electronic resource] by Geder, L Kreider, J W Towfighi, J Page, R B Ladda, R L Brennan, R W Rapp, F Producer: 19880105 In: Journal of neuro-oncology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestations. [electronic resource] by Robins, D B Ladda, R L Thieme, G A Boal, D K Emanuel, B S Zackai, E H Producer: 19890630 In: American journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Hereditary factors in sleepwalking and night terrors. [electronic resource] by Kales, A Soldatos, C R Bixler, E O Ladda, R L Charney, D S Weber, G Schweitzer, P K Producer: 19810116 In: The British journal of psychiatry : the journal of mental science vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia. [electronic resource] by Rogan, P K Close, P Blouin, J L Seip, J R Gannutz, L Ladda, R L Antonarakis, S E Producer: 19960327 In: American journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Three new point mutations in type II procollagen (COL2A1) and identification of a fourth family with the COL2A1 Arg519-->Cys base substitution using conformation sensitive gel electrophoresis. [electronic resource] by Williams, C J Rock, M Considine, E McCarron, S Gow, P Ladda, R McLain, D Michels, V M Murphy, W Prockop, D J Producer: 19950629 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. [electronic resource] by Puffenberger, E G Kauffman, E R Bolk, S Matise, T C Washington, S S Angrist, M Weissenbach, J Garver, K L Mascari, M Ladda, R Producer: 19950110 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. [electronic resource] by Mascari, M J Gottlieb, W Rogan, P K Butler, M G Waller, D A Armour, J A Jeffreys, A J Ladda, R L Nicholls, R D Producer: 19920616 In: The New England journal of medicine vol. 326 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Clinical and molecular analyses of deletion 3p25-pter syndrome. [electronic resource] by Mowrey, P N Chorney, M J Venditti, C P Latif, F Modi, W S Lerman, M I Zbar, B Robins, D B Rogan, P K Ladda, R L Producer: 19930930 In: American journal of medical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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