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W Wertelecki

Showing results (71-80 of 85) with videos related to

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American Journal of Obstetrics and Gynecology|March 15, 1981
Utilization of prenatal genetic diagnosis in women 35 years of age and older in the United States, 1977 to 1978M M Adams, S Finley, H Hansen, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 16, 2009
Can prenatal ultrasound detect the effects of in-utero alcohol exposure? A pilot studyM Kfir, L Yevtushok, S Onishchenko, et al.
American Journal of Human Genetics|February 1, 1990
Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22G A Rouleau, B R Seizinger, W Wertelecki, et al.
The New England Journal of Medicine|August 4, 1988
Neurofibromatosis 2: clinical and DNA linkage studies of a large kindredW Wertelecki, G A Rouleau, D W Superneau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panelC M Tuck-Muller, B K Goodman, S Li, et al.
American Journal of Human Genetics|August 1, 1992
Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagenL T Smith, W Wertelecki, L M Milstone, et al.
Biofactors (Oxford, England)|March 25, 2010
The plausibility of maternal nutritional status being a contributing factor to the risk for fetal alcohol spectrum disorders: the potential influence of zinc status as an exampleCarl L Keen, Janet Y Uriu-Adams, Anatoly Skalny, et al.
Human Genetics|July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literatureC M Tuck-Muller, H Chen, J E Martínez, et al.
Neurology|September 1, 1993
Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markersM H Ruttledge, S A Narod, J P Dumanski, et al.
Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Obstetrics and Gynecology|March 15, 1981
Utilization of prenatal genetic diagnosis in women 35 years of age and older in the United States, 1977 to 1978M M Adams, S Finley, H Hansen, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 16, 2009
Can prenatal ultrasound detect the effects of in-utero alcohol exposure? A pilot studyM Kfir, L Yevtushok, S Onishchenko, et al.
American Journal of Human Genetics|February 1, 1990
Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22G A Rouleau, B R Seizinger, W Wertelecki, et al.
The New England Journal of Medicine|August 4, 1988
Neurofibromatosis 2: clinical and DNA linkage studies of a large kindredW Wertelecki, G A Rouleau, D W Superneau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panelC M Tuck-Muller, B K Goodman, S Li, et al.
American Journal of Human Genetics|August 1, 1992
Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagenL T Smith, W Wertelecki, L M Milstone, et al.
Biofactors (Oxford, England)|March 25, 2010
The plausibility of maternal nutritional status being a contributing factor to the risk for fetal alcohol spectrum disorders: the potential influence of zinc status as an exampleCarl L Keen, Janet Y Uriu-Adams, Anatoly Skalny, et al.
Human Genetics|July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literatureC M Tuck-Muller, H Chen, J E Martínez, et al.
Neurology|September 1, 1993
Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markersM H Ruttledge, S A Narod, J P Dumanski, et al.
Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.
Pageof 9