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	1.	Early puberty in Williams syndrome. [electronic resource] by Cherniske, E M Sadler, L S Schwartz, D Carpenter, T O Pober, B R Producer: 19990628 In: Clinical dysmorphology vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	2.	46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters. [electronic resource] by Hisama, F M Zemel, S Cherniske, E M Vladutiu, G D Pober, B R Producer: 20010426 In: American journal of medical genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Truncating mutations in FOXC2 cause multiple lymphedema syndromes. [electronic resource] by Finegold, D N Kimak, M A Lawrence, E C Levinson, K L Cherniske, E M Pober, B R Dunlap, J W Ferrell, R E Producer: 20010816 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome? [electronic resource] by Jonsson, J J Renieri, A Gallagher, P G Kashtan, C E Cherniske, E M Bruttini, M Piccini, M Vitelli, F Ballabio, A Pober, B R Producer: 19980630 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy. [electronic resource] by Brown, C A Lanning, R W McKinney, K Q Salvino, A R Cherniske, E Crowe, C A Darras, B T Gominak, S Greenberg, C R Grosmann, C Heydemann, P Mendell, J R Pober, B R Sasaki, T Shapiro, F Simpson, D A Suchowersky, O Spence, J E Producer: 20011025 In: American journal of medical genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)