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Journal of Gerontology
|
March 1, 1983
A longitudinal study of nutritional intake in men
V K Elahi, D Elahi, R Andres, et al.
Human Molecular Genetics
|
April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient
Y Sun, R D Nicholls, M G Butler, et al.
Journal of Medical Genetics
|
March 19, 2002
Omphalocele in three generations with autosomal dominant transmission
S L Kanagawa, M L Begleiter, D J Ostlie, et al.
American Journal of Human Genetics
|
August 1, 1989
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5
J Overhauser, U Bengtsson, J McMahon, et al.
American Journal of Medical Genetics
|
January 1, 1991
An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene
E W Roback, A J Barakat, V G Dev, et al.
Journal of Clinical Pathology
|
May 1, 1986
Identification of immunoreactive atrial natriuretic peptide in atrial amyloid
G C Kaye, M G Butler, A J D'Ardenne, et al.
American Journal of Medical Genetics
|
December 1, 1988
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis
M G Butler, V G Dev, D Shah, et al.
The British Journal of Ophthalmology
|
August 1, 1992
Fibronectin synthesis in subretinal membranes of proliferative vitreoretinopathy
P Hiscott, H A Waller, I Grierson, et al.
American Journal of Medical Genetics
|
May 8, 2000
Metacarpophalangeal pattern profile analysis in Noonan syndrome
M G Butler, R Kumar, M F Davis, et al.
Radiology
|
July 1, 1995
Meniscal ossicle: radiographic and MR imaging findings
P Schnarkowski, P F Tirman, K D Fuchigami, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 212) with videos related to
Sort By:
Page
of 22
Journal of Gerontology
|
March 1, 1983
A longitudinal study of nutritional intake in men
V K Elahi, D Elahi, R Andres, et al.
Human Molecular Genetics
|
April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient
Y Sun, R D Nicholls, M G Butler, et al.
Journal of Medical Genetics
|
March 19, 2002
Omphalocele in three generations with autosomal dominant transmission
S L Kanagawa, M L Begleiter, D J Ostlie, et al.
American Journal of Human Genetics
|
August 1, 1989
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5
J Overhauser, U Bengtsson, J McMahon, et al.
American Journal of Medical Genetics
|
January 1, 1991
An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene
E W Roback, A J Barakat, V G Dev, et al.
Journal of Clinical Pathology
|
May 1, 1986
Identification of immunoreactive atrial natriuretic peptide in atrial amyloid
G C Kaye, M G Butler, A J D'Ardenne, et al.
American Journal of Medical Genetics
|
December 1, 1988
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis
M G Butler, V G Dev, D Shah, et al.
The British Journal of Ophthalmology
|
August 1, 1992
Fibronectin synthesis in subretinal membranes of proliferative vitreoretinopathy
P Hiscott, H A Waller, I Grierson, et al.
American Journal of Medical Genetics
|
May 8, 2000
Metacarpophalangeal pattern profile analysis in Noonan syndrome
M G Butler, R Kumar, M F Davis, et al.
Radiology
|
July 1, 1995
Meniscal ossicle: radiographic and MR imaging findings
P Schnarkowski, P F Tirman, K D Fuchigami, et al.
Page
of 22