Search research articles
Contact Us
Filters
Showing results (21-30 of 38) with videos related to
Page
of 4
Sort By:
Clinical Genetics
|
December 1, 1976
Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1
K L Garver, A M Ciocco, N A Turack
Clinical Genetics
|
December 1, 1987
Unusual pedigree patterns in families with spinal muscular atrophy
A E Lin, K L Garver, H Wessel, et al.
American Journal of Human Genetics
|
March 1, 1990
A genetic study of Hirschsprung disease
J A Badner, W K Sieber, K L Garver, et al.
Birth Defects Original Article Series
|
January 1, 1982
Midtrimester diagnosis of osteogenesis imperfecta, type II
N D Dinno, U A Yacoub, J F Kadlec, et al.
The Journal of Pediatrics
|
February 1, 1982
Recurrence risk in 21q/21q translocation of Down syndrome
K L Garver, S G Marchese, M W Steele, et al.
American Journal of Obstetrics and Gynecology
|
June 1, 1978
Reproductive outcome in a family with an inherited deletion-insertion chromosome 1
K L Garver, S G Marchese, S R Fatora, et al.
Enzyme
|
January 1, 1980
Origin of lactate dehydrogenase in amniotic fluid
K L Garver, S G Marchese, A E Wineman, et al.
Humangenetik
|
January 1, 1973
Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases
M F Niermeijer, D Halley, E Sachs, et al.
Clinical Genetics
|
April 1, 1981
Increased amnionic fluid alpha-fetoprotein due to a holoacardium amorphous twin
J H Harger, N Doshi, S Marchese, et al.
American Journal of Medical Genetics
|
November 1, 1988
Case of Pallister-Killian syndrome with imperforate anus
A E Lin, M Clemens, K L Garver, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 4
Clinical Genetics
|
December 1, 1976
Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1
K L Garver, A M Ciocco, N A Turack
Clinical Genetics
|
December 1, 1987
Unusual pedigree patterns in families with spinal muscular atrophy
A E Lin, K L Garver, H Wessel, et al.
American Journal of Human Genetics
|
March 1, 1990
A genetic study of Hirschsprung disease
J A Badner, W K Sieber, K L Garver, et al.
Birth Defects Original Article Series
|
January 1, 1982
Midtrimester diagnosis of osteogenesis imperfecta, type II
N D Dinno, U A Yacoub, J F Kadlec, et al.
The Journal of Pediatrics
|
February 1, 1982
Recurrence risk in 21q/21q translocation of Down syndrome
K L Garver, S G Marchese, M W Steele, et al.
American Journal of Obstetrics and Gynecology
|
June 1, 1978
Reproductive outcome in a family with an inherited deletion-insertion chromosome 1
K L Garver, S G Marchese, S R Fatora, et al.
Enzyme
|
January 1, 1980
Origin of lactate dehydrogenase in amniotic fluid
K L Garver, S G Marchese, A E Wineman, et al.
Humangenetik
|
January 1, 1973
Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases
M F Niermeijer, D Halley, E Sachs, et al.
Clinical Genetics
|
April 1, 1981
Increased amnionic fluid alpha-fetoprotein due to a holoacardium amorphous twin
J H Harger, N Doshi, S Marchese, et al.
American Journal of Medical Genetics
|
November 1, 1988
Case of Pallister-Killian syndrome with imperforate anus
A E Lin, M Clemens, K L Garver, et al.
Page
of 4