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Lancet (London, England)
|
October 14, 1989
Non-mosaic trisomy 16 confined to villi
M S Verp, B Rosinsky, Z Sheikh, et al.
Human Genetics
|
January 1, 1980
A ring 14 chromosome with deleted short arm
A P Amarose, E Dorus, P R Huttenlocher, et al.
American Journal of Obstetrics and Gynecology
|
April 15, 1977
Clinical, pathologic, and genetic findings in a case of 46,XY pure gonadal dysgenesis (Swyer's syndrome). II. Presence of H-Y antigen
E Dorus, A P Amarose, G C Koo, et al.
American Journal of Medical Genetics
|
July 1, 1989
Cystic hygroma and 45,X/46,XY mosaicism
M S Verp, Z Sheikh, A P Amarose, et al.
American Journal of Medical Genetics
|
January 1, 1987
Mosaic trisomy 7 and renal dysplasia
M S Verp, A P Amarose, J R Esterly, et al.
Human Genetics
|
January 1, 1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome
A P Amarose, P R Huttenlocher, R M Sprudzs, et al.
Clinical Genetics
|
October 1, 1979
A reciprocal translocation (X;11) in a female with gonadal dysgenesis
E Dorus, A P Amarose, D R Tredway, et al.
Fertility and Sterility
|
February 1, 1992
Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite
M S Verp, H H Harrison, C Ober, et al.
Science (New York, N.Y.)
|
May 6, 1977
H-y antigen: expression in human subjects with the testicular feminization syndrome
G C Koo, S S Wachtel, P Saenger, et al.
Teratology
|
January 1, 1990
Unique anomalies in cephalothoracopagus janiceps conjoined twins with implications for multiple mechanisms in the abnormal embryogenesis
B W Baron, D W Shermeta, M A Ismail, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Lancet (London, England)
|
October 14, 1989
Non-mosaic trisomy 16 confined to villi
M S Verp, B Rosinsky, Z Sheikh, et al.
Human Genetics
|
January 1, 1980
A ring 14 chromosome with deleted short arm
A P Amarose, E Dorus, P R Huttenlocher, et al.
American Journal of Obstetrics and Gynecology
|
April 15, 1977
Clinical, pathologic, and genetic findings in a case of 46,XY pure gonadal dysgenesis (Swyer's syndrome). II. Presence of H-Y antigen
E Dorus, A P Amarose, G C Koo, et al.
American Journal of Medical Genetics
|
July 1, 1989
Cystic hygroma and 45,X/46,XY mosaicism
M S Verp, Z Sheikh, A P Amarose, et al.
American Journal of Medical Genetics
|
January 1, 1987
Mosaic trisomy 7 and renal dysplasia
M S Verp, A P Amarose, J R Esterly, et al.
Human Genetics
|
January 1, 1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome
A P Amarose, P R Huttenlocher, R M Sprudzs, et al.
Clinical Genetics
|
October 1, 1979
A reciprocal translocation (X;11) in a female with gonadal dysgenesis
E Dorus, A P Amarose, D R Tredway, et al.
Fertility and Sterility
|
February 1, 1992
Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite
M S Verp, H H Harrison, C Ober, et al.
Science (New York, N.Y.)
|
May 6, 1977
H-y antigen: expression in human subjects with the testicular feminization syndrome
G C Koo, S S Wachtel, P Saenger, et al.
Teratology
|
January 1, 1990
Unique anomalies in cephalothoracopagus janiceps conjoined twins with implications for multiple mechanisms in the abnormal embryogenesis
B W Baron, D W Shermeta, M A Ismail, et al.
Page
of 2