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American Journal of Medical Genetics
|
April 1, 1988
Overgrowth, congenital hypotonia, nystagmus, strabismus, and mental retardation: variant of dominantly inherited Sotos sequence?
D J Goldstein, R E Ward, E Moore, et al.
American Journal of Perinatology
|
April 1, 1985
Lactation and phenylketonuria
N C Bradburn, R S Wappner, J A Lemons, et al.
The New England Journal of Medicine
|
June 19, 1986
Mevalonic aciduria--an inborn error of cholesterol and nonsterol isoprene biosynthesis
G Hoffmann, K M Gibson, I K Brandt, et al.
Radiology
|
June 1, 1995
Chiari I malformation: association with hypophosphatemic rickets and MR imaging appearance
K S Caldemeyer, J C Boaz, R S Wappner, et al.
Human Genetics
|
October 1, 1986
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature
M J Pettenati, J L Haines, R R Higgins, et al.
Clinical Genetics
|
October 1, 1977
7q deletion syndrome (7q32 leads to 7qter)
E L Harris, R S Wappner, C G Palmer, et al.
Clinical Genetics
|
August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six families
J M Vance, P M Conneally, R S Wappner, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiency
K M Gibson, R S Wappner, S Jooste, et al.
Journal of Pediatric Surgery
|
January 1, 1990
Peritoneal dialysis in the first 60 days of life
D E Matthews, K W West, F J Rescorla, et al.
American Journal of Medical Genetics
|
January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphism
J M Vance, M A Pericak-Vance, R C Elston, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
April 1, 1988
Overgrowth, congenital hypotonia, nystagmus, strabismus, and mental retardation: variant of dominantly inherited Sotos sequence?
D J Goldstein, R E Ward, E Moore, et al.
American Journal of Perinatology
|
April 1, 1985
Lactation and phenylketonuria
N C Bradburn, R S Wappner, J A Lemons, et al.
The New England Journal of Medicine
|
June 19, 1986
Mevalonic aciduria--an inborn error of cholesterol and nonsterol isoprene biosynthesis
G Hoffmann, K M Gibson, I K Brandt, et al.
Radiology
|
June 1, 1995
Chiari I malformation: association with hypophosphatemic rickets and MR imaging appearance
K S Caldemeyer, J C Boaz, R S Wappner, et al.
Human Genetics
|
October 1, 1986
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature
M J Pettenati, J L Haines, R R Higgins, et al.
Clinical Genetics
|
October 1, 1977
7q deletion syndrome (7q32 leads to 7qter)
E L Harris, R S Wappner, C G Palmer, et al.
Clinical Genetics
|
August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six families
J M Vance, P M Conneally, R S Wappner, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiency
K M Gibson, R S Wappner, S Jooste, et al.
Journal of Pediatric Surgery
|
January 1, 1990
Peritoneal dialysis in the first 60 days of life
D E Matthews, K W West, F J Rescorla, et al.
American Journal of Medical Genetics
|
January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphism
J M Vance, M A Pericak-Vance, R C Elston, et al.
Page
of 3