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American Journal of Medical Genetics
|
November 1, 1990
Malformations and minor anomalies in children whose mothers had prenatal diagnosis: comparison between CVS and amniocentesis
P Kaplan, J Normandin, G N Wilson, et al.
American Journal of Human Genetics
|
November 1, 1980
HeLa cell identification by analysis of ribosomal DNA segment patterns generated by endonuclease restriction
R D Schmickel, J R Waterson, M Knoller, et al.
Human Genetics
|
February 1, 1990
Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization
U Müller, N R Schneider, J F Marks, et al.
The Journal of Biological Chemistry
|
November 25, 1975
Cell-free transcription of mammalian chromatin. Quantitative measurement of newly synthesized globin messenger RNA sequences
G N Wilson, A W Steggles, J A Kantor, et al.
Clinical Genetics
|
April 1, 1994
Multiple coagulation defects and the Cohen syndrome
T L Schlichtemeier, G E Tomlinson, B A Kamen, et al.
American Journal of Medical Genetics
|
March 15, 1991
Balanced translocation 12/13 and situs abnormalities: homology of early pattern formation in man and lower organisms?
G N Wilson, J P Stout, N R Schneider, et al.
Gene
|
December 1, 1981
Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments
J M Erickson, C L Rushford, D J Dorney, et al.
Transplantation
|
November 1, 1985
Karyotypic chimerism and rejection in a pancreaticoduodenosplenic transplant
D C Dafoe, D A Campbell, W H Marks, et al.
American Journal of Medical Genetics
|
December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy
V Tonk, R A Schultz, S L Christian, et al.
The Journal of Pediatrics
|
April 1, 1983
Holoprosencephaly in infants of diabetic mothers
M Barr, J W Hanson, K Currey, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 88) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
November 1, 1990
Malformations and minor anomalies in children whose mothers had prenatal diagnosis: comparison between CVS and amniocentesis
P Kaplan, J Normandin, G N Wilson, et al.
American Journal of Human Genetics
|
November 1, 1980
HeLa cell identification by analysis of ribosomal DNA segment patterns generated by endonuclease restriction
R D Schmickel, J R Waterson, M Knoller, et al.
Human Genetics
|
February 1, 1990
Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization
U Müller, N R Schneider, J F Marks, et al.
The Journal of Biological Chemistry
|
November 25, 1975
Cell-free transcription of mammalian chromatin. Quantitative measurement of newly synthesized globin messenger RNA sequences
G N Wilson, A W Steggles, J A Kantor, et al.
Clinical Genetics
|
April 1, 1994
Multiple coagulation defects and the Cohen syndrome
T L Schlichtemeier, G E Tomlinson, B A Kamen, et al.
American Journal of Medical Genetics
|
March 15, 1991
Balanced translocation 12/13 and situs abnormalities: homology of early pattern formation in man and lower organisms?
G N Wilson, J P Stout, N R Schneider, et al.
Gene
|
December 1, 1981
Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments
J M Erickson, C L Rushford, D J Dorney, et al.
Transplantation
|
November 1, 1985
Karyotypic chimerism and rejection in a pancreaticoduodenosplenic transplant
D C Dafoe, D A Campbell, W H Marks, et al.
American Journal of Medical Genetics
|
December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy
V Tonk, R A Schultz, S L Christian, et al.
The Journal of Pediatrics
|
April 1, 1983
Holoprosencephaly in infants of diabetic mothers
M Barr, J W Hanson, K Currey, et al.
Page
of 9