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K L Garver

Showing results (21-30 of 38) with videos related to

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Clinical Genetics|December 1, 1976
Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1K L Garver, A M Ciocco, N A Turack
Clinical Genetics|December 1, 1987
Unusual pedigree patterns in families with spinal muscular atrophyA E Lin, K L Garver, H Wessel, et al.
American Journal of Human Genetics|March 1, 1990
A genetic study of Hirschsprung diseaseJ A Badner, W K Sieber, K L Garver, et al.
Birth Defects Original Article Series|January 1, 1982
Midtrimester diagnosis of osteogenesis imperfecta, type IIN 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 syndromeK 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 1K L Garver, S G Marchese, S R Fatora, et al.
Enzyme|January 1, 1980
Origin of lactate dehydrogenase in amniotic fluidK 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 diseasesM F Niermeijer, D Halley, E Sachs, et al.
Clinical Genetics|April 1, 1981
Increased amnionic fluid alpha-fetoprotein due to a holoacardium amorphous twinJ H Harger, N Doshi, S Marchese, et al.
American Journal of Medical Genetics|November 1, 1988
Case of Pallister-Killian syndrome with imperforate anusA E Lin, M Clemens, K L Garver, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Clinical Genetics|December 1, 1976
Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1K L Garver, A M Ciocco, N A Turack
Clinical Genetics|December 1, 1987
Unusual pedigree patterns in families with spinal muscular atrophyA E Lin, K L Garver, H Wessel, et al.
American Journal of Human Genetics|March 1, 1990
A genetic study of Hirschsprung diseaseJ A Badner, W K Sieber, K L Garver, et al.
Birth Defects Original Article Series|January 1, 1982
Midtrimester diagnosis of osteogenesis imperfecta, type IIN 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 syndromeK 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 1K L Garver, S G Marchese, S R Fatora, et al.
Enzyme|January 1, 1980
Origin of lactate dehydrogenase in amniotic fluidK 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 diseasesM F Niermeijer, D Halley, E Sachs, et al.
Clinical Genetics|April 1, 1981
Increased amnionic fluid alpha-fetoprotein due to a holoacardium amorphous twinJ H Harger, N Doshi, S Marchese, et al.
American Journal of Medical Genetics|November 1, 1988
Case of Pallister-Killian syndrome with imperforate anusA E Lin, M Clemens, K L Garver, et al.
Pageof 4