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J A Phillips

Showing results (191-200 of 197) with videos related to

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Human Biology|February 11, 1999
Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in BrazilS Raskin, J A Phillips, G Kaplan, et al.
Thorax|November 2, 2004
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPFW E Lawson, S W Grant, V Ambrosini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 5, 2001
Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trialA Amalfitano, A R Bengur, R P Morse, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
22q13.3 deletion syndrome: clinical and molecular analysis using array CGHS U Dhar, D del Gaudio, J R German, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 8, 2011
Vaginal progesterone reduces the rate of preterm birth in women with a sonographic short cervix: a multicenter, randomized, double-blind, placebo-controlled trialS S Hassan, R Romero, D Vidyadhari, et al.
Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.
Pageof 20

Showing results (191-200 of 197) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 197 results.
Human Biology|February 11, 1999
Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in BrazilS Raskin, J A Phillips, G Kaplan, et al.
Thorax|November 2, 2004
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPFW E Lawson, S W Grant, V Ambrosini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 5, 2001
Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trialA Amalfitano, A R Bengur, R P Morse, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
22q13.3 deletion syndrome: clinical and molecular analysis using array CGHS U Dhar, D del Gaudio, J R German, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 8, 2011
Vaginal progesterone reduces the rate of preterm birth in women with a sonographic short cervix: a multicenter, randomized, double-blind, placebo-controlled trialS S Hassan, R Romero, D Vidyadhari, et al.
Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.
Pageof 20