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Nucleic Acids Research
|
March 11, 1992
Dinucleotide repeat polymorphism at the D11S860 locus
L A McNoe, M R Eccles, A E Reeve
Clinical Genetics
|
May 1, 1997
Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies
R P Erickson, J F Stone, L A McNoe, et al.
Human Molecular Genetics
|
November 1, 1995
Mutation of PAX2 in two siblings with renal-coloboma syndrome
P Sanyanusin, L A McNoe, M J Sullivan, et al.
Human Molecular Genetics
|
December 1, 1993
Human insulin-like growth factor type I and type II receptors are not imprinted
O Ogawa, L A McNoe, M R Eccles, et al.
Journal of Medical Genetics
|
May 23, 1998
Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux
K L Choi, L A McNoe, M C French, et al.
Genomics
|
July 1, 1996
Genomic structure of the human PAX2 gene
P Sanyanusin, J H Norrish, T A Ward, et al.
Journal of Medical Genetics
|
October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies
H E Cunliffe, L A McNoe, T A Ward, et al.
The Journal of Pathology
|
May 20, 2008
Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes
R Fukuzawa, M R Anaka, R W Heathcott, et al.
Nature
|
April 22, 1993
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
O Ogawa, M R Eccles, J Szeto, et al.
Nature Genetics
|
April 1, 1995
Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
P Sanyanusin, L A Schimmenti, L A McNoe, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Nucleic Acids Research
|
March 11, 1992
Dinucleotide repeat polymorphism at the D11S860 locus
L A McNoe, M R Eccles, A E Reeve
Clinical Genetics
|
May 1, 1997
Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies
R P Erickson, J F Stone, L A McNoe, et al.
Human Molecular Genetics
|
November 1, 1995
Mutation of PAX2 in two siblings with renal-coloboma syndrome
P Sanyanusin, L A McNoe, M J Sullivan, et al.
Human Molecular Genetics
|
December 1, 1993
Human insulin-like growth factor type I and type II receptors are not imprinted
O Ogawa, L A McNoe, M R Eccles, et al.
Journal of Medical Genetics
|
May 23, 1998
Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux
K L Choi, L A McNoe, M C French, et al.
Genomics
|
July 1, 1996
Genomic structure of the human PAX2 gene
P Sanyanusin, J H Norrish, T A Ward, et al.
Journal of Medical Genetics
|
October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies
H E Cunliffe, L A McNoe, T A Ward, et al.
The Journal of Pathology
|
May 20, 2008
Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes
R Fukuzawa, M R Anaka, R W Heathcott, et al.
Nature
|
April 22, 1993
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
O Ogawa, M R Eccles, J Szeto, et al.
Nature Genetics
|
April 1, 1995
Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
P Sanyanusin, L A Schimmenti, L A McNoe, et al.
Page
of 2