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	1.	Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: heterogeneity or variable expressivity? [electronic resource] by Grebe, T A Clericuzio, C Producer: 19970225 In: American journal of medical genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype. [electronic resource] by Grebe, T A Clericuzio, C Producer: 20010104 In: American journal of medical genetics vol. 95 Availability: No items available. Save to lists Add to cart (remove)
	3.	Toxic reaction to salicylate in a newborn infant: similarities to neonatal sepsis. [electronic resource] by Buck, M L Grebe, T A Bond, G R Producer: 19930629 In: The Journal of pediatrics vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach. [electronic resource] by Aintablian, H K Narayanan, V Belnap, N Ramsey, K Grebe, T A Publication details: Molecular genetics and metabolism reports Mar 2017 In: Molecular genetics and metabolism reports vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	7p deletion syndrome: an adult with mild manifestations. [electronic resource] by Grebe, T A Stevens, M A Byrne-Essif, K Cassidy, S B Producer: 19921006 In: American journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Further delineation of the epidermal nevus syndrome: two cases with new findings and literature review. [electronic resource] by Grebe, T A Rimsza, M E Richter, S F Hansen, R C Hoyme, H E Producer: 19931007 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A rational approach to cystic fibrosis mutation analysis in Hispanics: reply to Arzimanoglou et al. [electronic resource] by Grebe, T A Doane, W W Richter, S F Seltzer, W K Jain, K D Producer: 19960801 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	8.	Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency. [electronic resource] by He, G Yang, B Z Roe, D S Teramoto, R Aleck, K Grebe, T A Roe, C R Ding, J H Producer: 19991207 In: Biochemical and biophysical research communications vol. 264 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection. [electronic resource] by Chen, Z Grebe, T A Guan, X Y Notohamiprodjo, M Nutting, P J Stone, J F Trent, J M Sandberg, A A Producer: 19970903 In: American journal of medical genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Complete detection of mutations in cystic fibrosis patients of Native American origin. [electronic resource] by Mercier, B Raguénès, O Estivill, X Morral, N Kaplan, G C McClure, M Grebe, T A Kessler, D Pignatti, P F Marigo, C Producer: 19950110 In: Human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome. [electronic resource] by Conroy, J M Grebe, T A Becker, L A Tsuchiya, K Nicholls, R D Buiting, K Horsthemke, B Cassidy, S B Schwartz, S Producer: 19971015 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutation analysis of the cystic fibrosis transmembrane regulator gene in Native American populations of the southwest. [electronic resource] by Grebe, T A Doane, W W Richter, S F Clericuzio, C Norman, R A Seltzer, W K Rhodes, S N Goldberg, B E Hernried, L S McClure, M Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	13.	Genetic analysis of Hispanic individuals with cystic fibrosis. [electronic resource] by Grebe, T A Seltzer, W K DeMarchi, J Silva, D K Doane, W W Gozal, D Richter, S F Bowman, C M Norman, R A Rhodes, S N Producer: 19940325 In: American journal of human genetics vol. 54 Availability: No items available. Save to lists Add to cart (remove)
	14.	22q13.3 deletion syndrome: clinical and molecular analysis using array CGH. [electronic resource] by Dhar, S U del Gaudio, D German, J R Peters, S U Ou, Z Bader, P I Berg, J S Blazo, M Brown, C W Graham, B H Grebe, T A Lalani, S Irons, M Sparagana, S Williams, M Phillips, J A Beaudet, A L Stankiewicz, P Patel, A Cheung, S W Sahoo, T Producer: 20100412 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)