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Trine Prescott

Showing results (1-10 of 38) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 1, 2016
Predictive testing should be in the child's best interestsTrine Prescott
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 24, 2013
A diagnostic revolutionTrine Prescott
European Journal of Medical Genetics|August 30, 2008
1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotypeOlaug K Rødningen, Trine Prescott, Ann-Sofie Eriksson, et al.
European Journal of Medical Genetics|November 4, 2010
Exon trapping analysis of c.301-19G > A in intron 1 of the SHH gene in a patient with a microform of holoprosencephalyMari Ann Kulseth, Robert Lyle, Olaug K Rødningen, et al.
Clinical Dysmorphology|September 15, 2004
Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEGArpad Matlary, Trine Prescott, Bjørn Tvedt, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 2020
Gene panel testingIda W Sørensen, Trine Prescott, Cecilie F Rustad, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2022
Prophylactic Allogeneic Hematopoietic Stem Cell Therapy for CSF1R-Related LeukoencephalopathyMorten Andreas Horn, Anders Eivind Myhre, Trine Prescott, et al.
European Journal of Medical Genetics|March 15, 2006
Focal preauricular dermal dysplasia: distinctive congenital lesions with a bilateral and symmetric distributionTrine Prescott, Koen Devriendt, Ben Hamel, et al.
European Journal of Medical Genetics|June 28, 2015
A Novel Oculo-Skeletal syndrome with intellectual disability caused by a particular MAB21L2 mutationDenise Horn, Trine Prescott, Gunnar Houge, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertionHelle Lybaek, Karen Helene Ørstavik, Trine Prescott, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 1, 2016
Predictive testing should be in the child's best interestsTrine Prescott
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 24, 2013
A diagnostic revolutionTrine Prescott
European Journal of Medical Genetics|August 30, 2008
1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotypeOlaug K Rødningen, Trine Prescott, Ann-Sofie Eriksson, et al.
European Journal of Medical Genetics|November 4, 2010
Exon trapping analysis of c.301-19G > A in intron 1 of the SHH gene in a patient with a microform of holoprosencephalyMari Ann Kulseth, Robert Lyle, Olaug K Rødningen, et al.
Clinical Dysmorphology|September 15, 2004
Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEGArpad Matlary, Trine Prescott, Bjørn Tvedt, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 2020
Gene panel testingIda W Sørensen, Trine Prescott, Cecilie F Rustad, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2022
Prophylactic Allogeneic Hematopoietic Stem Cell Therapy for CSF1R-Related LeukoencephalopathyMorten Andreas Horn, Anders Eivind Myhre, Trine Prescott, et al.
European Journal of Medical Genetics|March 15, 2006
Focal preauricular dermal dysplasia: distinctive congenital lesions with a bilateral and symmetric distributionTrine Prescott, Koen Devriendt, Ben Hamel, et al.
European Journal of Medical Genetics|June 28, 2015
A Novel Oculo-Skeletal syndrome with intellectual disability caused by a particular MAB21L2 mutationDenise Horn, Trine Prescott, Gunnar Houge, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertionHelle Lybaek, Karen Helene Ørstavik, Trine Prescott, et al.
Pageof 4