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David L Rimoin

Showing results (41-50 of 78) with videos related to

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American Journal of Medical Genetics. Part A|December 17, 2009
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2Areeg H El-Gharbawy, Joseph N Peeden, Ralph S Lachman, et al.
American Journal of Human Genetics|December 20, 2002
Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved geneDaniel H Cohn, Nadia Ehtesham, Deborah Krakow, et al.
Insights Into Imaging|February 21, 2012
The skeleton and musculature on foetal MRIUrsula Nemec, Stefan F Nemec, Deborah Krakow, et al.
Prenatal Diagnosis|April 13, 2012
Male genital abnormalities in intrauterine growth restrictionStefan F Nemec, Ursula Nemec, Peter C Brugger, et al.
Prenatal Diagnosis|March 21, 2012
MR imaging of the fetal musculoskeletal systemStefan Franz Nemec, Ursula Nemec, Peter C Brugger, et al.
Pediatric Radiology|April 24, 2003
Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic featuresStephen F Miller, Virginia K Proud, Alice L Werner, et al.
European Journal of Radiology|July 1, 2011
Situs anomalies on prenatal MRIStefan F Nemec, Peter C Brugger, Ursula Nemec, et al.
American Journal of Human Genetics|August 6, 2002
Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12Nadia Ehtesham, Rita M Cantor, Lily M King, et al.
Stem Cells and Development|February 25, 2014
Patient-derived skeletal dysplasia induced pluripotent stem cells display abnormal chondrogenic marker expression and regulation by BMP2 and TGFβ1Biagio Saitta, Jenna Passarini, Dhruv Sareen, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphologyAlison M Elliott, William R Wilcox, Gerald S Spear, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|December 17, 2009
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2Areeg H El-Gharbawy, Joseph N Peeden, Ralph S Lachman, et al.
American Journal of Human Genetics|December 20, 2002
Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved geneDaniel H Cohn, Nadia Ehtesham, Deborah Krakow, et al.
Insights Into Imaging|February 21, 2012
The skeleton and musculature on foetal MRIUrsula Nemec, Stefan F Nemec, Deborah Krakow, et al.
Prenatal Diagnosis|April 13, 2012
Male genital abnormalities in intrauterine growth restrictionStefan F Nemec, Ursula Nemec, Peter C Brugger, et al.
Prenatal Diagnosis|March 21, 2012
MR imaging of the fetal musculoskeletal systemStefan Franz Nemec, Ursula Nemec, Peter C Brugger, et al.
Pediatric Radiology|April 24, 2003
Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic featuresStephen F Miller, Virginia K Proud, Alice L Werner, et al.
European Journal of Radiology|July 1, 2011
Situs anomalies on prenatal MRIStefan F Nemec, Peter C Brugger, Ursula Nemec, et al.
American Journal of Human Genetics|August 6, 2002
Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12Nadia Ehtesham, Rita M Cantor, Lily M King, et al.
Stem Cells and Development|February 25, 2014
Patient-derived skeletal dysplasia induced pluripotent stem cells display abnormal chondrogenic marker expression and regulation by BMP2 and TGFβ1Biagio Saitta, Jenna Passarini, Dhruv Sareen, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphologyAlison M Elliott, William R Wilcox, Gerald S Spear, et al.
Pageof 8