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N B Kardon

Showing results (1-10 of 22) with videos related to

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Female Patient|November 1, 1991
Advancing maternal age: the actual risksJ L Chervenak, N B Kardon
Cancer Genetics and Cytogenetics|August 1, 1982
Childhood acute lymphoblastic leukemia associated with an unusual 8;14 translocationN B Kardon, G Slepowitz, J A Kochen
American Journal of Medical Genetics|March 10, 2001
Trisomy 1 in a clinically recognized IVF pregnancyT M Dunn, L Grunfeld, N B Kardon
The Journal of Pediatrics|March 1, 1977
Chromosomal mosaicism in amniotic fluid cell culturesN B Kardon, M Krauss, J G Davis, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|February 1, 1986
Antenatal diagnosis of frontal cephalocele in a fetus with atelosteogenesisF A Chervenak, G Isaacson, J C Rosenberg, et al.
Journal of Medical Genetics|December 1, 1983
De novo duplication of the 7q11 leads to q22 regionN B Kardon, L Pollack, J Davis, et al.
Clinical Genetics|March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicismN B Kardon, E Lieber, J G Davis, et al.
Human Genetics|February 1, 1980
Incidence of chromosomal rearrangements in couples with reproductive lossN B Kardon, J G Davis, A L Berger, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocationA L Shanske, L Edelmann, N B Kardon, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Female Patient|November 1, 1991
Advancing maternal age: the actual risksJ L Chervenak, N B Kardon
Cancer Genetics and Cytogenetics|August 1, 1982
Childhood acute lymphoblastic leukemia associated with an unusual 8;14 translocationN B Kardon, G Slepowitz, J A Kochen
American Journal of Medical Genetics|March 10, 2001
Trisomy 1 in a clinically recognized IVF pregnancyT M Dunn, L Grunfeld, N B Kardon
The Journal of Pediatrics|March 1, 1977
Chromosomal mosaicism in amniotic fluid cell culturesN B Kardon, M Krauss, J G Davis, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|February 1, 1986
Antenatal diagnosis of frontal cephalocele in a fetus with atelosteogenesisF A Chervenak, G Isaacson, J C Rosenberg, et al.
Journal of Medical Genetics|December 1, 1983
De novo duplication of the 7q11 leads to q22 regionN B Kardon, L Pollack, J Davis, et al.
Clinical Genetics|March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicismN B Kardon, E Lieber, J G Davis, et al.
Human Genetics|February 1, 1980
Incidence of chromosomal rearrangements in couples with reproductive lossN B Kardon, J G Davis, A L Berger, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocationA L Shanske, L Edelmann, N B Kardon, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.
Pageof 3