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N H Robin

Showing results (41-50 of 61) with videos related to

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American Journal of Human Genetics|November 4, 2000
Parental attitudes toward genetic testing for pediatric deafnessJ W Brunger, G S Murray, M O'Riordan, et al.
American Journal of Medical Genetics|March 13, 1995
Classical Noonan syndrome is not associated with deletions of 22q11N H Robin, B Sellinger, D McDonald-McGinn, et al.
Human Genetics|November 1, 1993
Human malformations similar to those in the mouse mutation disorganization (Ds)N H Robin, O O Adewale, D McDonald-McGinn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Molecular refinement of karyotype: beyond the cytogenetic bandD A Sirko-Osadsa, S B Cassidy, T W Depinet, et al.
The Journal of Pediatrics|November 5, 1997
Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndromeA D DePiero, E M Lourie, B W Berman, et al.
American Journal of Medical Genetics|November 15, 1994
Non-immune hydrops fetalis associated with impaired fetal movement: a case report and reviewN H Robin, M T Curtis, W Mulla, et al.
The Journal of Pediatrics|March 20, 1998
Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagenD A Sirko-Osadsa, M A Murray, J A Scott, et al.
American Journal of Medical Genetics|February 25, 1998
Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classificationN H Robin, J A Scott, J E Arnold, et al.
American Journal of Medical Genetics|January 2, 1996
Frontonasal malformation and cloacal exstrophy: a previously unreported associationN H Robin, J A Neidich, L D Bason, et al.
Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|November 4, 2000
Parental attitudes toward genetic testing for pediatric deafnessJ W Brunger, G S Murray, M O'Riordan, et al.
American Journal of Medical Genetics|March 13, 1995
Classical Noonan syndrome is not associated with deletions of 22q11N H Robin, B Sellinger, D McDonald-McGinn, et al.
Human Genetics|November 1, 1993
Human malformations similar to those in the mouse mutation disorganization (Ds)N H Robin, O O Adewale, D McDonald-McGinn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Molecular refinement of karyotype: beyond the cytogenetic bandD A Sirko-Osadsa, S B Cassidy, T W Depinet, et al.
The Journal of Pediatrics|November 5, 1997
Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndromeA D DePiero, E M Lourie, B W Berman, et al.
American Journal of Medical Genetics|November 15, 1994
Non-immune hydrops fetalis associated with impaired fetal movement: a case report and reviewN H Robin, M T Curtis, W Mulla, et al.
The Journal of Pediatrics|March 20, 1998
Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagenD A Sirko-Osadsa, M A Murray, J A Scott, et al.
American Journal of Medical Genetics|February 25, 1998
Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classificationN H Robin, J A Scott, J E Arnold, et al.
American Journal of Medical Genetics|January 2, 1996
Frontonasal malformation and cloacal exstrophy: a previously unreported associationN H Robin, J A Neidich, L D Bason, et al.
Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.
Pageof 7