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Prenatal Diagnosis
|
December 1, 1989
Alpha-fetoprotein and acetylcholinesterase in twins discordant for neural tube defect
V P Johnson, J Vidgoff, N Wilson, et al.
American Journal of Medical Genetics
|
December 1, 1991
Pelizaeus-Merzbacher disease: clinical and DNA-linkage study of an extended family
V P Johnson, N J Carpenter, K A Kelts
American Journal of Medical Genetics
|
July 1, 1983
A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism
V P Johnson, J M McMillin, T Aceto, et al.
American Journal of Medical Genetics
|
April 1, 1991
Sex chromosome marker: clinical significance and DNA characterization
V P Johnson, P G McDonough, S W Cheung, et al.
Birth Defects Original Article Series
|
January 1, 1982
Midtrimester prenatal diagnosis of short-limb dwarfism (Saldino-Noonan syndrome)
V P Johnson, L P Petersen, D R Holzwarth, et al.
American Journal of Medical Genetics
|
February 2, 1996
Fetal alcohol syndrome: craniofacial and central nervous system manifestations
V P Johnson, I I Swayze VW, Y Sato, et al.
American Journal of Medical Genetics
|
August 1, 1994
FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site
V P Johnson, M R Altherr, J M Blake, et al.
American Journal of Medical Genetics
|
December 1, 1985
Deletion of the distal long arm of chromosome 1: a definable syndrome
V P Johnson, L J Heck, G A Carter, et al.
South Dakota Journal of Medicine
|
July 1, 1996
Familial breast cancer risk assessment
V P Johnson, C A Storm, P Skorey-Solberg, et al.
American Journal of Medical Genetics
|
September 15, 1992
Natural history of mosaic trisomy 14 syndrome
A Fujimoto, J Allanson, C A Crowe, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 45) with videos related to
Sort By:
Page
of 5
Prenatal Diagnosis
|
December 1, 1989
Alpha-fetoprotein and acetylcholinesterase in twins discordant for neural tube defect
V P Johnson, J Vidgoff, N Wilson, et al.
American Journal of Medical Genetics
|
December 1, 1991
Pelizaeus-Merzbacher disease: clinical and DNA-linkage study of an extended family
V P Johnson, N J Carpenter, K A Kelts
American Journal of Medical Genetics
|
July 1, 1983
A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism
V P Johnson, J M McMillin, T Aceto, et al.
American Journal of Medical Genetics
|
April 1, 1991
Sex chromosome marker: clinical significance and DNA characterization
V P Johnson, P G McDonough, S W Cheung, et al.
Birth Defects Original Article Series
|
January 1, 1982
Midtrimester prenatal diagnosis of short-limb dwarfism (Saldino-Noonan syndrome)
V P Johnson, L P Petersen, D R Holzwarth, et al.
American Journal of Medical Genetics
|
February 2, 1996
Fetal alcohol syndrome: craniofacial and central nervous system manifestations
V P Johnson, I I Swayze VW, Y Sato, et al.
American Journal of Medical Genetics
|
August 1, 1994
FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site
V P Johnson, M R Altherr, J M Blake, et al.
American Journal of Medical Genetics
|
December 1, 1985
Deletion of the distal long arm of chromosome 1: a definable syndrome
V P Johnson, L J Heck, G A Carter, et al.
South Dakota Journal of Medicine
|
July 1, 1996
Familial breast cancer risk assessment
V P Johnson, C A Storm, P Skorey-Solberg, et al.
American Journal of Medical Genetics
|
September 15, 1992
Natural history of mosaic trisomy 14 syndrome
A Fujimoto, J Allanson, C A Crowe, et al.
Page
of 5