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L I Gardner

Showing results (61-70 of 112) with videos related to

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Journal of Medical Genetics|December 1, 1971
A case of 48,XXY,21+ in an infant with Down's syndromeR L Neu, A Q Scheuer, L I Gardner
JAMA|December 4, 1972
Nondisjunction in males: commoner than suspected?D A Lynch, R I Neu, L I Gardner
The Journal of Pediatrics|September 1, 1972
History may reveal more than growth hormone levelsM J Barlow, L I Gardner, S D Frasier
Clinical Genetics|August 1, 1977
A t(5p-;21q+) translocation in a family with Down syndromeR L Neu, F V DeGeorge, L I Gardner
Journal of Medical Genetics|June 1, 1971
47,XX,13+ with Snodgrass phenotype II. Are different chromosomes associated with two clinical varieties of D-trisomy?R L Neu, S R Assemany, L I Gardner
Clinical Genetics|January 1, 1973
A case of 46,XY,5(3q-;14q+)MatR L Neu, M J Barlow, L I Gardner
Fertility and Sterility|October 1, 1973
Communications and commentaries: A 46,XYq- male with aspermiaR L Neu, M J Barlow, L I Gardner
Archives of Environmental Health|May 1, 1972
Lack of damage to human chromosomes and dimethyl mercuryD Kasputis, R L Neu, L I Gardner, et al.
The New England Journal of Medicine|November 26, 1970
Lack of chromosome aberrations in autismM Wolraich, B Bzostek, R L Neu, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1970
An adult phenotypic male with a 46,XX chromosome complementH O Powers, R L Neu, H Smulyan, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Journal of Medical Genetics|December 1, 1971
A case of 48,XXY,21+ in an infant with Down's syndromeR L Neu, A Q Scheuer, L I Gardner
JAMA|December 4, 1972
Nondisjunction in males: commoner than suspected?D A Lynch, R I Neu, L I Gardner
The Journal of Pediatrics|September 1, 1972
History may reveal more than growth hormone levelsM J Barlow, L I Gardner, S D Frasier
Clinical Genetics|August 1, 1977
A t(5p-;21q+) translocation in a family with Down syndromeR L Neu, F V DeGeorge, L I Gardner
Journal of Medical Genetics|June 1, 1971
47,XX,13+ with Snodgrass phenotype II. Are different chromosomes associated with two clinical varieties of D-trisomy?R L Neu, S R Assemany, L I Gardner
Clinical Genetics|January 1, 1973
A case of 46,XY,5(3q-;14q+)MatR L Neu, M J Barlow, L I Gardner
Fertility and Sterility|October 1, 1973
Communications and commentaries: A 46,XYq- male with aspermiaR L Neu, M J Barlow, L I Gardner
Archives of Environmental Health|May 1, 1972
Lack of damage to human chromosomes and dimethyl mercuryD Kasputis, R L Neu, L I Gardner, et al.
The New England Journal of Medicine|November 26, 1970
Lack of chromosome aberrations in autismM Wolraich, B Bzostek, R L Neu, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1970
An adult phenotypic male with a 46,XX chromosome complementH O Powers, R L Neu, H Smulyan, et al.
Pageof 12