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E W Reich

Showing results (1-10 of 5) with videos related to

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Birth Defects Original Article Series|January 1, 1977
Interdisciplinary education in clinical geneticsR P Cox, E W Reich, J B Cox
American Journal of Human Genetics|August 1, 1987
Spontaneous mutation and parental age in humansN Risch, E W Reich, M M Wishnick, et al.
Birth Defects Original Article Series|January 1, 1978
Recognition in adult patients of malformations induced by folic-acid antagonistsE W Reich, R P Cox, M H Becker, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Birth Defects Original Article Series|January 1, 1977
Interdisciplinary education in clinical geneticsR P Cox, E W Reich, J B Cox
American Journal of Human Genetics|August 1, 1987
Spontaneous mutation and parental age in humansN Risch, E W Reich, M M Wishnick, et al.
Birth Defects Original Article Series|January 1, 1978
Recognition in adult patients of malformations induced by folic-acid antagonistsE W Reich, R P Cox, M H Becker, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Pageof 1