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L Wenger

Showing results (91-100 of 221) with videos related to

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American Journal of Medical Genetics|May 16, 1997
Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromesS L Wenger, S L Sell, M J Painter, et al.
International Journal of Surgical Pathology|May 30, 2008
Del(5q) is associated with clinical and histological parameters in small cell neuroendocrine lung carcinomaPaul H Hartel, Amy L Shackelford, James V Hartel, et al.
Teratology|February 1, 1987
Anatomical defects associated with a feathering mutant (Ottawa naked) in domestic fowlJ E Fulton, B S Wenger, E L Wenger, et al.
Clinical Genetics|July 1, 1986
Relative reliability of three different discriminant analysis methods for detecting PKU gene carriersS L Wenger, P W Vieira, J M Breck, et al.
American Journal of Medical Genetics. Part A|January 12, 2021
41st Annual David W. Smith workshop on malformations and morphogenesis: Abstracts of the 2020 annual meetingKaren W Gripp, Kenneth Lyons Jones, Tara L Wenger, et al.
Prenatal Diagnosis|September 5, 2002
Maternal cell contamination in an amniotic fluid sampleSallie L McAdoo, O C Bleigh, G Millard Simmons, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1989
The fragile X marker and autism in perspectiveJ B Payton, M W Steele, S L Wenger, et al.
The American Journal of Emergency Medicine|March 11, 1991
Results of multicenter studies of digoxin-specific antibody fragments in managing digitalis intoxication in the pediatric populationA D Woolf, T L Wenger, T W Smith, et al.
Cardiology Clinics|May 1, 1983
Sinus node dysfunctionC R Kerr, A O Grant, T L Wenger, et al.
Clinical Genetics|January 1, 1984
The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1M W Steele, S L Wenger, L O Geweke, et al.
Pageof 23

Showing results (91-100 of 221) with videos related to

Sort By:
Pageof 23
American Journal of Medical Genetics|May 16, 1997
Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromesS L Wenger, S L Sell, M J Painter, et al.
International Journal of Surgical Pathology|May 30, 2008
Del(5q) is associated with clinical and histological parameters in small cell neuroendocrine lung carcinomaPaul H Hartel, Amy L Shackelford, James V Hartel, et al.
Teratology|February 1, 1987
Anatomical defects associated with a feathering mutant (Ottawa naked) in domestic fowlJ E Fulton, B S Wenger, E L Wenger, et al.
Clinical Genetics|July 1, 1986
Relative reliability of three different discriminant analysis methods for detecting PKU gene carriersS L Wenger, P W Vieira, J M Breck, et al.
American Journal of Medical Genetics. Part A|January 12, 2021
41st Annual David W. Smith workshop on malformations and morphogenesis: Abstracts of the 2020 annual meetingKaren W Gripp, Kenneth Lyons Jones, Tara L Wenger, et al.
Prenatal Diagnosis|September 5, 2002
Maternal cell contamination in an amniotic fluid sampleSallie L McAdoo, O C Bleigh, G Millard Simmons, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1989
The fragile X marker and autism in perspectiveJ B Payton, M W Steele, S L Wenger, et al.
The American Journal of Emergency Medicine|March 11, 1991
Results of multicenter studies of digoxin-specific antibody fragments in managing digitalis intoxication in the pediatric populationA D Woolf, T L Wenger, T W Smith, et al.
Cardiology Clinics|May 1, 1983
Sinus node dysfunctionC R Kerr, A O Grant, T L Wenger, et al.
Clinical Genetics|January 1, 1984
The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1M W Steele, S L Wenger, L O Geweke, et al.
Pageof 23