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D W Superneau

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Pediatric Cardiology|January 18, 2003
Unusual cardiac malformations in conjoined twins: thoracopagus twins with conjoined pentalogy of Cantrell and an omphalopagus twin with atretic ventriclesR Spencer, W H Robichaux, D W Superneau, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 1, 1996
Aberrant retropharyngeal internal carotid artery in a child with spondyloepimetaphyseal dysplasia and cleft palateM M Fluke, D R Bronfin, D W Superneau, et al.
American Journal of Medical Genetics|October 1, 1993
Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndromeS R Braddock, K L Jones, D W Superneau, et al.
Clinical Genetics|July 11, 2012
Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotypeN Hoppman-Chaney, K Wain, P R Seger, et al.
Birth Defects Original Article Series|January 1, 1982
Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 casesW R Blackburn, W P Miller, D W Superneau, 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.
American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, 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.
Nature|September 17, 1987
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22G A Rouleau, W Wertelecki, J L Haines, et al.
American Journal of Medical Genetics|July 31, 2001
Meier-Gorlin syndrome: report of eight additional cases and reviewE M Bongers, J M Opitz, A Fryer, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Pediatric Cardiology|January 18, 2003
Unusual cardiac malformations in conjoined twins: thoracopagus twins with conjoined pentalogy of Cantrell and an omphalopagus twin with atretic ventriclesR Spencer, W H Robichaux, D W Superneau, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 1, 1996
Aberrant retropharyngeal internal carotid artery in a child with spondyloepimetaphyseal dysplasia and cleft palateM M Fluke, D R Bronfin, D W Superneau, et al.
American Journal of Medical Genetics|October 1, 1993
Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndromeS R Braddock, K L Jones, D W Superneau, et al.
Clinical Genetics|July 11, 2012
Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotypeN Hoppman-Chaney, K Wain, P R Seger, et al.
Birth Defects Original Article Series|January 1, 1982
Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 casesW R Blackburn, W P Miller, D W Superneau, 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.
American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, 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.
Nature|September 17, 1987
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22G A Rouleau, W Wertelecki, J L Haines, et al.
American Journal of Medical Genetics|July 31, 2001
Meier-Gorlin syndrome: report of eight additional cases and reviewE M Bongers, J M Opitz, A Fryer, et al.
Pageof 2