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Female Patient
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November 1, 1991
Advancing maternal age: the actual risks
J L Chervenak, N B Kardon
Cancer Genetics and Cytogenetics
|
August 1, 1982
Childhood acute lymphoblastic leukemia associated with an unusual 8;14 translocation
N B Kardon, G Slepowitz, J A Kochen
American Journal of Medical Genetics
|
March 10, 2001
Trisomy 1 in a clinically recognized IVF pregnancy
T M Dunn, L Grunfeld, N B Kardon
The Journal of Pediatrics
|
March 1, 1977
Chromosomal mosaicism in amniotic fluid cell cultures
N 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 atelosteogenesis
F 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 region
N B Kardon, L Pollack, J Davis, et al.
Clinical Genetics
|
March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicism
N B Kardon, E Lieber, J G Davis, et al.
Human Genetics
|
February 1, 1980
Incidence of chromosomal rearrangements in couples with reproductive loss
N 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 translocation
A 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.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Female Patient
|
November 1, 1991
Advancing maternal age: the actual risks
J L Chervenak, N B Kardon
Cancer Genetics and Cytogenetics
|
August 1, 1982
Childhood acute lymphoblastic leukemia associated with an unusual 8;14 translocation
N B Kardon, G Slepowitz, J A Kochen
American Journal of Medical Genetics
|
March 10, 2001
Trisomy 1 in a clinically recognized IVF pregnancy
T M Dunn, L Grunfeld, N B Kardon
The Journal of Pediatrics
|
March 1, 1977
Chromosomal mosaicism in amniotic fluid cell cultures
N 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 atelosteogenesis
F 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 region
N B Kardon, L Pollack, J Davis, et al.
Clinical Genetics
|
March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicism
N B Kardon, E Lieber, J G Davis, et al.
Human Genetics
|
February 1, 1980
Incidence of chromosomal rearrangements in couples with reproductive loss
N 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 translocation
A 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.
Page
of 3