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Showing results (101-110 of 107) with videos related to

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American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidismB T Teh, S Kytölä, F Farnebo, 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|October 26, 2000
9th international workshop on fragile X syndrome and X-linked mental retardationJ P Fryns, M Borghgraef, T W Brown, et al.
American Journal of Human Genetics|September 16, 1999
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.
American Journal of Human Genetics|January 3, 2001
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyC Gaspar, I Lopes-Cendes, S Hayes, et al.
American Journal of Human Genetics|December 12, 2000
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and IIIH J Lüdecke, J Schaper, P Meinecke, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 107 results.
American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidismB T Teh, S Kytölä, F Farnebo, 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|October 26, 2000
9th international workshop on fragile X syndrome and X-linked mental retardationJ P Fryns, M Borghgraef, T W Brown, et al.
American Journal of Human Genetics|September 16, 1999
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.
American Journal of Human Genetics|January 3, 2001
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyC Gaspar, I Lopes-Cendes, S Hayes, et al.
American Journal of Human Genetics|December 12, 2000
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and IIIH J Lüdecke, J Schaper, P Meinecke, et al.
Pageof 11