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K A Leppig

Showing results (1-10 of 20) with videos related to

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Clinical Dysmorphology|October 1, 1993
Phenotypic correlations of ocular coloboma without known causeK A Leppig, R A Pagon
Seminars in Reproductive Medicine|August 2, 2001
Ring X and other structural X chromosome abnormalities: X inactivation and phenotypeK A Leppig, C M Disteche
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Cloning of the human homolog of the CDC34 cell cycle gene by complementation in yeastS E Plon, K A Leppig, H N Do, et al.
American Journal of Medical Genetics|August 18, 2000
Familial cryptic (20;21) translocation identified by in situ hybridization technologiesK A Leppig, S Ball, K Au, et al.
American Journal of Medical Genetics|December 31, 1997
Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromataK A Leppig, P Kaplan, D Viskochil, et al.
Clinical Dysmorphology|April 18, 1998
Brachydactyly type A1 with abnormal menisci and scoliosis in three generationsM L Raff, K A Leppig, J C Rutledge, et al.
American Journal of Medical Genetics|October 28, 1996
Trisomy 10p: report of an unusual mechanism of formation and critical evaluation of the clinical phenotypeS J Clement, K A Leppig, G P Jarvik, et al.
American Journal of Diseases of Children (1960)|December 1, 1988
Minor malformations: significant or insignificantK A Leppig, M M Werler, C I Cann, et al.
The Journal of Pediatrics|April 1, 1987
Predictive value of minor anomalies. I. Association with major malformationsK A Leppig, M M Werler, C I Cann, et al.
Journal of Medical Genetics|May 19, 2001
The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndromeM A Parisi, M B Dinulos, K A Leppig, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Clinical Dysmorphology|October 1, 1993
Phenotypic correlations of ocular coloboma without known causeK A Leppig, R A Pagon
Seminars in Reproductive Medicine|August 2, 2001
Ring X and other structural X chromosome abnormalities: X inactivation and phenotypeK A Leppig, C M Disteche
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Cloning of the human homolog of the CDC34 cell cycle gene by complementation in yeastS E Plon, K A Leppig, H N Do, et al.
American Journal of Medical Genetics|August 18, 2000
Familial cryptic (20;21) translocation identified by in situ hybridization technologiesK A Leppig, S Ball, K Au, et al.
American Journal of Medical Genetics|December 31, 1997
Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromataK A Leppig, P Kaplan, D Viskochil, et al.
Clinical Dysmorphology|April 18, 1998
Brachydactyly type A1 with abnormal menisci and scoliosis in three generationsM L Raff, K A Leppig, J C Rutledge, et al.
American Journal of Medical Genetics|October 28, 1996
Trisomy 10p: report of an unusual mechanism of formation and critical evaluation of the clinical phenotypeS J Clement, K A Leppig, G P Jarvik, et al.
American Journal of Diseases of Children (1960)|December 1, 1988
Minor malformations: significant or insignificantK A Leppig, M M Werler, C I Cann, et al.
The Journal of Pediatrics|April 1, 1987
Predictive value of minor anomalies. I. Association with major malformationsK A Leppig, M M Werler, C I Cann, et al.
Journal of Medical Genetics|May 19, 2001
The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndromeM A Parisi, M B Dinulos, K A Leppig, et al.
Pageof 2