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C O Leonard

Showing results (31-40 of 35) with videos related to

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Journal of Developmental and Behavioral Pediatrics : JDBP|August 1, 1996
Children and adolescents with neurofibromatosis 1: a behavioral phenotypeC V Dilts, J C Carey, J C Kircher, et al.
The Journal of Pediatrics|April 1, 1983
Respiratory complications of achondroplasiaD C Stokes, J A Phillips, C O Leonard, et al.
American Journal of Human Genetics|July 1, 1995
Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patientsM C Lowery, C A Morris, A Ewart, et al.
American Journal of Medical Genetics|January 1, 1989
Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndromeJ S Bamforth, C O Leonard, B N Chodirker, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Developmental and Behavioral Pediatrics : JDBP|August 1, 1996
Children and adolescents with neurofibromatosis 1: a behavioral phenotypeC V Dilts, J C Carey, J C Kircher, et al.
The Journal of Pediatrics|April 1, 1983
Respiratory complications of achondroplasiaD C Stokes, J A Phillips, C O Leonard, et al.
American Journal of Human Genetics|July 1, 1995
Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patientsM C Lowery, C A Morris, A Ewart, et al.
American Journal of Medical Genetics|January 1, 1989
Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndromeJ S Bamforth, C O Leonard, B N Chodirker, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
Pageof 4