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M S Lubinsky

Showing results (21-30 of 29) with videos related to

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American Journal of Medical Genetics|May 1, 1984
Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndromeJ K Stern, M S Lubinsky, D S Durrie, et al.
Journal of Clinical and Experimental Neuropsychology|January 19, 1999
A further report on a case of Floating-Harbor Syndrome in a mother and daughterA C Rosen, R F Newby, C M Sauer, et al.
American Journal of Medical Genetics|March 1, 1987
Cat-eye syndrome with different marker chromosomes in a mother and daughterP S Ing, M S Lubinsky, S D Smith, et al.
American Journal of Medical Genetics|September 1, 1994
von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomaliesM S Lubinsky, S G Kahler, I E Speer, et al.
Acta Dermato-Venereologica|December 1, 1993
GM1-gangliosidosis type 1 involving the cutaneous vascular endothelial cells in a black infant with multiple ectopic Mongolian spotsT T Tang, N B Esterly, M S Lubinsky, et al.
American Journal of Human Genetics|July 1, 1993
Minimum guidelines for the delivery of clinical genetics services. The Evaluation of Clinical Services Subcommittee, Great Lakes Regional Genetics GroupD D Weaver, D Baker, M Theobald, et al.
Acta Neuropathologica|January 1, 1994
Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosisT T Tang, A D Segura, Y T Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.
Human Genetics|May 1, 1996
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathyB B Roa, F Greenberg, P Gunaratne, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
American Journal of Medical Genetics|May 1, 1984
Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndromeJ K Stern, M S Lubinsky, D S Durrie, et al.
Journal of Clinical and Experimental Neuropsychology|January 19, 1999
A further report on a case of Floating-Harbor Syndrome in a mother and daughterA C Rosen, R F Newby, C M Sauer, et al.
American Journal of Medical Genetics|March 1, 1987
Cat-eye syndrome with different marker chromosomes in a mother and daughterP S Ing, M S Lubinsky, S D Smith, et al.
American Journal of Medical Genetics|September 1, 1994
von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomaliesM S Lubinsky, S G Kahler, I E Speer, et al.
Acta Dermato-Venereologica|December 1, 1993
GM1-gangliosidosis type 1 involving the cutaneous vascular endothelial cells in a black infant with multiple ectopic Mongolian spotsT T Tang, N B Esterly, M S Lubinsky, et al.
American Journal of Human Genetics|July 1, 1993
Minimum guidelines for the delivery of clinical genetics services. The Evaluation of Clinical Services Subcommittee, Great Lakes Regional Genetics GroupD D Weaver, D Baker, M Theobald, et al.
Acta Neuropathologica|January 1, 1994
Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosisT T Tang, A D Segura, Y T Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.
Human Genetics|May 1, 1996
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathyB B Roa, F Greenberg, P Gunaratne, et al.
Pageof 3