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American Journal of Medical Genetics
|
September 5, 1997
Growth hormone insufficiency associated with haploinsufficiency at 18q23
J D Cody, D E Hale, Z Brkanac, et al.
Human Genetics
|
December 22, 1999
Haplosufficiency of the melancortin-4 receptor gene in individuals with deletions of 18q
J D Cody, X T Reveles, D E Hale, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 3, 2001
The spectrum of growth abnormalities in children with 18q deletions
D E Hale, J D Cody, J Baillargeon, et al.
American Journal of Medical Genetics
|
March 31, 1997
Preferential loss of the paternal alleles in the 18q- syndrome
J D Cody, J F Pierce, Z Brkanac, et al.
American Journal of Human Genetics
|
November 5, 1997
Genetic linkage of Paget disease of the bone to chromosome 18q
J D Cody, F R Singer, G D Roodman, et al.
The Cochrane Database of Systematic Reviews
|
July 22, 2005
Cellulose, modified cellulose and synthetic membranes in the haemodialysis of patients with end-stage renal disease
A M Macleod, M Campbell, J D Cody, et al.
American Journal of Medical Genetics
|
April 29, 1998
Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss
K M Keppler-Noreuil, A J Carroll, S C Finley, et al.
American Journal of Medical Genetics
|
March 3, 1997
Growth hormone deficiency associated in the 18q deletion syndrome
P D Ghidoni, D E Hale, J D Cody, et al.
American Journal of Medical Genetics
|
June 8, 2001
Genetic mapping of a novel X-linked recessive colobomatous microphthalmia
D M Lehman, W E Sponsel, R F Stratton, et al.
American Journal of Medical Genetics
|
July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q
J D Cody, P D Ghidoni, B R DuPont, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
September 5, 1997
Growth hormone insufficiency associated with haploinsufficiency at 18q23
J D Cody, D E Hale, Z Brkanac, et al.
Human Genetics
|
December 22, 1999
Haplosufficiency of the melancortin-4 receptor gene in individuals with deletions of 18q
J D Cody, X T Reveles, D E Hale, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 3, 2001
The spectrum of growth abnormalities in children with 18q deletions
D E Hale, J D Cody, J Baillargeon, et al.
American Journal of Medical Genetics
|
March 31, 1997
Preferential loss of the paternal alleles in the 18q- syndrome
J D Cody, J F Pierce, Z Brkanac, et al.
American Journal of Human Genetics
|
November 5, 1997
Genetic linkage of Paget disease of the bone to chromosome 18q
J D Cody, F R Singer, G D Roodman, et al.
The Cochrane Database of Systematic Reviews
|
July 22, 2005
Cellulose, modified cellulose and synthetic membranes in the haemodialysis of patients with end-stage renal disease
A M Macleod, M Campbell, J D Cody, et al.
American Journal of Medical Genetics
|
April 29, 1998
Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss
K M Keppler-Noreuil, A J Carroll, S C Finley, et al.
American Journal of Medical Genetics
|
March 3, 1997
Growth hormone deficiency associated in the 18q deletion syndrome
P D Ghidoni, D E Hale, J D Cody, et al.
American Journal of Medical Genetics
|
June 8, 2001
Genetic mapping of a novel X-linked recessive colobomatous microphthalmia
D M Lehman, W E Sponsel, R F Stratton, et al.
American Journal of Medical Genetics
|
July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q
J D Cody, P D Ghidoni, B R DuPont, et al.
Page
of 3