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Journal of Cell Science
|
December 1, 1992
Molecular characterization of the secondary constriction region (qh) of human chromosome 9 with pericentric inversion
S Luke, R S Verma, R A Conte, et al.
Gynecologic and Obstetric Investigation
|
January 1, 1994
Monozygotic twinning in a female with triple X[47,XXX]
R S Verma, R A Conte, T Mathews, et al.
Genetic Analysis, Techniques and Applications
|
October 1, 1992
Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16
R S Verma, S Luke, T Mathews, et al.
Human Heredity
|
May 1, 1993
Chromosomal anomalies in 1,000 children referred with suspected genetic disorders
D Navsaria, T Mathews, R A Conte, et al.
The Japanese Journal of Human Genetics
|
December 1, 1994
An apparent balanced translocation between chromosomes 7 and 13 [t(7;13)(p15;q32)] in a 47,XYY individual
R S Verma, R Giridharan, R A Conte, et al.
Clinical Genetics
|
February 1, 1992
The interstitial deletion of bands q33-35 of long arm of chromosome 7: a review with a new case report
R S Verma, R A Conte, S E Sayegh, et al.
Clinical Genetics
|
March 1, 1997
Delineation of a ring chromosome 16 by the FISH-technique: a case report with review
R A Conte, S M Kleyman, C Kharode, et al.
Clinical Genetics
|
August 1, 1996
Molecular characterization of 21p- variant chromosome
R A Conte, T Mathews, S M Kleyman, et al.
Journal of Medical Genetics
|
January 1, 1992
Pericentric inversion of chromosome 7 (inv(7) (p22q11.2)) and ring chromosome 8 (r(8) (p23q24.3)) in a girl with minor anomalies
R S Verma, R A Conte, J H Pitter, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
December 1, 1987
Physical signs and symptoms in preschool-age hyperactive and normal children
B J Kaplan, J McNicol, R A Conte, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 58) with videos related to
Sort By:
Page
of 6
Journal of Cell Science
|
December 1, 1992
Molecular characterization of the secondary constriction region (qh) of human chromosome 9 with pericentric inversion
S Luke, R S Verma, R A Conte, et al.
Gynecologic and Obstetric Investigation
|
January 1, 1994
Monozygotic twinning in a female with triple X[47,XXX]
R S Verma, R A Conte, T Mathews, et al.
Genetic Analysis, Techniques and Applications
|
October 1, 1992
Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16
R S Verma, S Luke, T Mathews, et al.
Human Heredity
|
May 1, 1993
Chromosomal anomalies in 1,000 children referred with suspected genetic disorders
D Navsaria, T Mathews, R A Conte, et al.
The Japanese Journal of Human Genetics
|
December 1, 1994
An apparent balanced translocation between chromosomes 7 and 13 [t(7;13)(p15;q32)] in a 47,XYY individual
R S Verma, R Giridharan, R A Conte, et al.
Clinical Genetics
|
February 1, 1992
The interstitial deletion of bands q33-35 of long arm of chromosome 7: a review with a new case report
R S Verma, R A Conte, S E Sayegh, et al.
Clinical Genetics
|
March 1, 1997
Delineation of a ring chromosome 16 by the FISH-technique: a case report with review
R A Conte, S M Kleyman, C Kharode, et al.
Clinical Genetics
|
August 1, 1996
Molecular characterization of 21p- variant chromosome
R A Conte, T Mathews, S M Kleyman, et al.
Journal of Medical Genetics
|
January 1, 1992
Pericentric inversion of chromosome 7 (inv(7) (p22q11.2)) and ring chromosome 8 (r(8) (p23q24.3)) in a girl with minor anomalies
R S Verma, R A Conte, J H Pitter, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
December 1, 1987
Physical signs and symptoms in preschool-age hyperactive and normal children
B J Kaplan, J McNicol, R A Conte, et al.
Page
of 6