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E Haan

Showing results (31-40 of 61) with videos related to

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Clinical Genetics|December 25, 2004
The Hunter-McAlpine syndrome results from duplication 5q35-qterA G W Hunter, B Dupont, M McLaughlin, et al.
Paediatric and Perinatal Epidemiology|April 30, 2005
A South Australian population-based study of congenital talipes equinovarusR Byron-Scott, P Sharpe, C Hasler, et al.
Experimental Neurology|November 26, 2003
SUMO-1 marks the nuclear inclusions in familial neuronal intranuclear inclusion diseaseD L Pountney, Y Huang, R J Burns, et al.
Journal of Paediatrics and Child Health|October 1, 1995
Hydrometrocolpos and segmental colonic dilatation in a girl with megacystis-microcolon-intestinal hypoperistalsis syndromeP A Dewan, N Brown, D P Murthy, et al.
Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.
American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.
Journal of Medical Genetics|February 1, 1996
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletionA Smith, C Wiles, E Haan, et al.
The American Surgeon|April 25, 2000
Human endothelial cell cultures from progenitor cells obtained by leukapheresisD A Hernandez, L E Townsend, M R Uzieblo, et al.
Clinical Genetics|August 6, 2011
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC geneR Nagy, H Wang, B Albrecht, et al.
The Journal of Pediatrics|June 1, 1987
Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical casesK Hayasaka, K Tada, N Fueki, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Clinical Genetics|December 25, 2004
The Hunter-McAlpine syndrome results from duplication 5q35-qterA G W Hunter, B Dupont, M McLaughlin, et al.
Paediatric and Perinatal Epidemiology|April 30, 2005
A South Australian population-based study of congenital talipes equinovarusR Byron-Scott, P Sharpe, C Hasler, et al.
Experimental Neurology|November 26, 2003
SUMO-1 marks the nuclear inclusions in familial neuronal intranuclear inclusion diseaseD L Pountney, Y Huang, R J Burns, et al.
Journal of Paediatrics and Child Health|October 1, 1995
Hydrometrocolpos and segmental colonic dilatation in a girl with megacystis-microcolon-intestinal hypoperistalsis syndromeP A Dewan, N Brown, D P Murthy, et al.
Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.
American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.
Journal of Medical Genetics|February 1, 1996
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletionA Smith, C Wiles, E Haan, et al.
The American Surgeon|April 25, 2000
Human endothelial cell cultures from progenitor cells obtained by leukapheresisD A Hernandez, L E Townsend, M R Uzieblo, et al.
Clinical Genetics|August 6, 2011
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC geneR Nagy, H Wang, B Albrecht, et al.
The Journal of Pediatrics|June 1, 1987
Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical casesK Hayasaka, K Tada, N Fueki, et al.
Pageof 7