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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1993
[The natural history of syndromes with a metabolic origin]
G Andria
Human Molecular Genetics
|
July 1, 1992
Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses
A Ballabio, G Andria
The Journal of Biological Chemistry
|
April 10, 1978
The complementing fragment-dependent renaturation by enzyme-catalyzed disulfide interchanges of RNase-(1-118) containing non-native disulfide bonds
G Andria, H Taniuchi
American Journal of Medical Genetics
|
March 10, 2001
Congenital insensitivity to pain with anhidrosis: an NGF/TrkA-related disorder
E Toscano, G Andria
Pediatric Research
|
January 1, 1981
Intermediate golgi alpha-D-mannosidosis and mucolipidosis II and III
G Andria, W S Sly
Human Genetics
|
December 15, 1976
Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome
M C Silengo, G Andria
Archives of Disease in Childhood
|
August 23, 2001
Cholelithiasis in Down's syndrome
E Toscano, V Trivellini, G Andria
Annals of Neurology
|
January 1, 1988
More on X-linked ichthyosis, steroid sulfatase deficiency, and hypogonadism and anosmia
G Andria, A Ballabio, G Parenti
Biochimica Et Biophysica Acta
|
January 8, 1976
Alpha-Glutamyl-beta-naphthylamide hydrolase of rabbit small intestine. Localization in the brush border and separation from other brush border peptidases
G Andria, A Marzi, S Auricchio
Annals of Neurology
|
July 1, 1987
X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia
G Andria, A Ballabio, G Parenti
Page
of 14
Search research articles
Search
Showing results (1-10 of 137) with videos related to
Sort By:
Page
of 14
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1993
[The natural history of syndromes with a metabolic origin]
G Andria
Human Molecular Genetics
|
July 1, 1992
Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses
A Ballabio, G Andria
The Journal of Biological Chemistry
|
April 10, 1978
The complementing fragment-dependent renaturation by enzyme-catalyzed disulfide interchanges of RNase-(1-118) containing non-native disulfide bonds
G Andria, H Taniuchi
American Journal of Medical Genetics
|
March 10, 2001
Congenital insensitivity to pain with anhidrosis: an NGF/TrkA-related disorder
E Toscano, G Andria
Pediatric Research
|
January 1, 1981
Intermediate golgi alpha-D-mannosidosis and mucolipidosis II and III
G Andria, W S Sly
Human Genetics
|
December 15, 1976
Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome
M C Silengo, G Andria
Archives of Disease in Childhood
|
August 23, 2001
Cholelithiasis in Down's syndrome
E Toscano, V Trivellini, G Andria
Annals of Neurology
|
January 1, 1988
More on X-linked ichthyosis, steroid sulfatase deficiency, and hypogonadism and anosmia
G Andria, A Ballabio, G Parenti
Biochimica Et Biophysica Acta
|
January 8, 1976
Alpha-Glutamyl-beta-naphthylamide hydrolase of rabbit small intestine. Localization in the brush border and separation from other brush border peptidases
G Andria, A Marzi, S Auricchio
Annals of Neurology
|
July 1, 1987
X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia
G Andria, A Ballabio, G Parenti
Page
of 14