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American Journal of Medical Genetics
|
January 1, 1979
Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease
B R Elejalde, J Holguin, A Valencia, et al.
Wisconsin Medical Journal
|
February 1, 1994
DNA testing and genetic counseling: truth or consequences
N C Reynolds, R R Lebel, K de S Hamsher, et al.
Human Genetics
|
January 1, 1981
H-Y antigen expression in a case of mixed gonadal dysgenesis
C A Moreira-Filho, A T Amaral, P G Otto, et al.
Birth Defects Original Article Series
|
January 1, 1977
The pallister mosaic syndrome
P D Pallister, L F Meisner, B R Elejalde, et al.
American Journal of Medical Genetics
|
April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies
B R Elejalde, J M Opitz, M M de Elejalde, et al.
American Journal of Human Genetics
|
April 3, 2001
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans
B K Jordan, M Mohammed, S T Ching, et al.
Nuclear Medicine Communications
|
December 19, 2001
Single photon emission computerized tomography (SPECT) in detecting neurodegeneration in Huntington's disease
N C Reynolds, R S Hellman, R S Tikofsky, et al.
American Journal of Medical Genetics
|
April 17, 1998
A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes
G Dewald, R Stallard, A Al Saadi, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
American Journal of Medical Genetics
|
January 1, 1979
Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease
B R Elejalde, J Holguin, A Valencia, et al.
Wisconsin Medical Journal
|
February 1, 1994
DNA testing and genetic counseling: truth or consequences
N C Reynolds, R R Lebel, K de S Hamsher, et al.
Human Genetics
|
January 1, 1981
H-Y antigen expression in a case of mixed gonadal dysgenesis
C A Moreira-Filho, A T Amaral, P G Otto, et al.
Birth Defects Original Article Series
|
January 1, 1977
The pallister mosaic syndrome
P D Pallister, L F Meisner, B R Elejalde, et al.
American Journal of Medical Genetics
|
April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies
B R Elejalde, J M Opitz, M M de Elejalde, et al.
American Journal of Human Genetics
|
April 3, 2001
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans
B K Jordan, M Mohammed, S T Ching, et al.
Nuclear Medicine Communications
|
December 19, 2001
Single photon emission computerized tomography (SPECT) in detecting neurodegeneration in Huntington's disease
N C Reynolds, R S Hellman, R S Tikofsky, et al.
American Journal of Medical Genetics
|
April 17, 1998
A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes
G Dewald, R Stallard, A Al Saadi, et al.
Page
of 5