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Human Biology
|
February 11, 1999
Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil
S 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 IPF
W 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 trial
A 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 hypertension
R 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 CGH
S 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 trial
S 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 study
S E Antonarakis, J P Rossiter, M Young, et al.
Page
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Search research articles
Search
Showing results (191-200 of 197) with videos related to
Sort By:
Page
of 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 Brazil
S 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 IPF
W 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 trial
A 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 hypertension
R 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 CGH
S 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 trial
S 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 study
S E Antonarakis, J P Rossiter, M Young, et al.
Page
of 20