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Molecular Genetics and Metabolism
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January 4, 2001
Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia
Y P Conley, D N Finegold, D G Peters, et al.
Pediatric Research
|
May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies
R Ziadeh, E P Hoffman, D N Finegold, et al.
Human Molecular Genetics
|
November 18, 1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneity
R E Ferrell, K L Levinson, J H Esman, et al.
Pediatric Research
|
September 1, 1994
Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13
D N Finegold, M M Armitage, M Galiani, et al.
Nature Genetics
|
June 3, 2000
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
M J Karkkainen, R E Ferrell, E C Lawrence, et al.
Reproduction (Cambridge, England)
|
May 30, 2003
Maternal and fetal amino acid concentrations and fetal outcomes during pre-eclampsia
R W Evans, R W Powers, R B Ness, et al.
Human Molecular Genetics
|
May 24, 2001
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
D N Finegold, M A Kimak, E C Lawrence, et al.
Orthodontics & Craniofacial Research
|
July 21, 2011
The effects of testosterone on craniosynostotic calvarial cells: a test of the gene/environmental model of craniofacial anomalies
J J Cray, E L Durham, M A Smalley, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
April 9, 2001
VEGFR3 gene structure, regulatory region, and sequence polymorphisms
K Iljin, M J Karkkainen, E C Lawrence, et al.
American Journal of Diseases of Children (1960)
|
May 1, 1992
Effect of somatotropin of mammalian cell origin in growth hormone deficiency
S D Frasier, C R Rudlin, H J Zeisel, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Molecular Genetics and Metabolism
|
January 4, 2001
Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia
Y P Conley, D N Finegold, D G Peters, et al.
Pediatric Research
|
May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies
R Ziadeh, E P Hoffman, D N Finegold, et al.
Human Molecular Genetics
|
November 18, 1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneity
R E Ferrell, K L Levinson, J H Esman, et al.
Pediatric Research
|
September 1, 1994
Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13
D N Finegold, M M Armitage, M Galiani, et al.
Nature Genetics
|
June 3, 2000
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
M J Karkkainen, R E Ferrell, E C Lawrence, et al.
Reproduction (Cambridge, England)
|
May 30, 2003
Maternal and fetal amino acid concentrations and fetal outcomes during pre-eclampsia
R W Evans, R W Powers, R B Ness, et al.
Human Molecular Genetics
|
May 24, 2001
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
D N Finegold, M A Kimak, E C Lawrence, et al.
Orthodontics & Craniofacial Research
|
July 21, 2011
The effects of testosterone on craniosynostotic calvarial cells: a test of the gene/environmental model of craniofacial anomalies
J J Cray, E L Durham, M A Smalley, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
April 9, 2001
VEGFR3 gene structure, regulatory region, and sequence polymorphisms
K Iljin, M J Karkkainen, E C Lawrence, et al.
American Journal of Diseases of Children (1960)
|
May 1, 1992
Effect of somatotropin of mammalian cell origin in growth hormone deficiency
S D Frasier, C R Rudlin, H J Zeisel, et al.
Page
of 4