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M W Steele

Showing results (31-40 of 68) with videos related to

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In Vitro|August 1, 1981
Incorporation of bacteriophage DNA into the genome of cultured human lymphocytesS L Wenger, M W Steele, J H Turner
Clinical Genetics|July 1, 1979
A patient with a 47,XXY,5p- karyotypeS Palevsky, N Radfar, S Pan, et al.
The Journal of Pediatrics|August 1, 1978
Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformationsD M Kurnit, M W Steele, L Pinsky, et al.
Clinical Genetics|February 1, 1983
A simplified PKU gene carrier detection test using fasting bloodB Tenenholz, S L Wenger, J Breck, et al.
The Journal of Pediatrics|November 1, 1973
Monosomy of chromosome No. 22. A case reportF DeCicco, M W Steele, S Pan, et al.
Clinical Genetics|October 1, 1986
Effect of sibship position on reproductive behavior of couples after the birth of a genetically handicapped childM W Steele, L Rosser, J B Rodnan, et al.
American Journal of Medical Genetics|March 13, 1995
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocationJ A Scott, S L Wenger, M W Steele, et al.
Pediatric Radiology|January 1, 1984
Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostosesR Dominguez, L W Young, M W Steele, et al.
Clinical Genetics|August 1, 1984
Prader-Willi syndrome in black femalesW L Golden, J M Hanchett, N Breslin, et al.
Clinical Genetics|April 1, 1997
Terminal 2q deletion--a recognizable syndromeS L Wenger, L Y Boone, U Surti, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
In Vitro|August 1, 1981
Incorporation of bacteriophage DNA into the genome of cultured human lymphocytesS L Wenger, M W Steele, J H Turner
Clinical Genetics|July 1, 1979
A patient with a 47,XXY,5p- karyotypeS Palevsky, N Radfar, S Pan, et al.
The Journal of Pediatrics|August 1, 1978
Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformationsD M Kurnit, M W Steele, L Pinsky, et al.
Clinical Genetics|February 1, 1983
A simplified PKU gene carrier detection test using fasting bloodB Tenenholz, S L Wenger, J Breck, et al.
The Journal of Pediatrics|November 1, 1973
Monosomy of chromosome No. 22. A case reportF DeCicco, M W Steele, S Pan, et al.
Clinical Genetics|October 1, 1986
Effect of sibship position on reproductive behavior of couples after the birth of a genetically handicapped childM W Steele, L Rosser, J B Rodnan, et al.
American Journal of Medical Genetics|March 13, 1995
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocationJ A Scott, S L Wenger, M W Steele, et al.
Pediatric Radiology|January 1, 1984
Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostosesR Dominguez, L W Young, M W Steele, et al.
Clinical Genetics|August 1, 1984
Prader-Willi syndrome in black femalesW L Golden, J M Hanchett, N Breslin, et al.
Clinical Genetics|April 1, 1997
Terminal 2q deletion--a recognizable syndromeS L Wenger, L Y Boone, U Surti, et al.
Pageof 7