Search research articles
Contact Us
Filters
Showing results (11-20 of 53) with videos related to
Page
of 6
Sort By:
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
December 4, 2024
Non-genetic diagnostic investigations in monogenic Ehlers-Danlos syndromes
Fleur S van Dijk, Chloe Angwin, Neeti Ghali, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
December 4, 2024
Clinical diagnosis of the monogenic Ehlers-Danlos syndromes
Fleur S van Dijk, Chloe Angwin, Serwet Demirdas, et al.
European Journal of Medical Genetics
|
August 1, 2017
Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis
Fleur S van Dijk, Grazia M S Mancini, Alessandra Maugeri, et al.
JAMA Dermatology
|
January 8, 2015
Atrophoderma Vermiculatum: A Cutaneous Feature of Loeys-Dietz Syndrome
Fleur S van Dijk, Helen Brittain, Ragna Boerma, et al.
Orphanet Journal of Rare Diseases
|
July 19, 2024
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification
Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, et al.
Bone
|
September 11, 2021
Fractures following pregnancy in Osteogenesis imperfecta - A self-controlled case series using Danish Health Registers
Emilie Karense Lykking, Heidi Kammerlander, Fleur S van Dijk, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
November 20, 2014
[A girl with Angelman syndrome]
Jan Maarten Cobben, Arjen van Hal, Nora van den Puttelaar-van Hal, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2019
Amniotic band sequence in paternal half-siblings with vascular Ehlers-Danlos syndrome
Mary B Callaghan, Rob Hadden, Jon S King, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2012
Clinical utility gene card for: osteogenesis imperfecta
Fleur S van Dijk, Raymond Dalgleish, Fransiska Malfait, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 24, 2012
[Osteogenesis imperfecta: clinical and genetic heterogeneity]
Fleur S van Dijk, Jan M Cobben, Alessandra Maugeri, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 53) with videos related to
Sort By:
Page
of 6
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
December 4, 2024
Non-genetic diagnostic investigations in monogenic Ehlers-Danlos syndromes
Fleur S van Dijk, Chloe Angwin, Neeti Ghali, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
December 4, 2024
Clinical diagnosis of the monogenic Ehlers-Danlos syndromes
Fleur S van Dijk, Chloe Angwin, Serwet Demirdas, et al.
European Journal of Medical Genetics
|
August 1, 2017
Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis
Fleur S van Dijk, Grazia M S Mancini, Alessandra Maugeri, et al.
JAMA Dermatology
|
January 8, 2015
Atrophoderma Vermiculatum: A Cutaneous Feature of Loeys-Dietz Syndrome
Fleur S van Dijk, Helen Brittain, Ragna Boerma, et al.
Orphanet Journal of Rare Diseases
|
July 19, 2024
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification
Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, et al.
Bone
|
September 11, 2021
Fractures following pregnancy in Osteogenesis imperfecta - A self-controlled case series using Danish Health Registers
Emilie Karense Lykking, Heidi Kammerlander, Fleur S van Dijk, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
November 20, 2014
[A girl with Angelman syndrome]
Jan Maarten Cobben, Arjen van Hal, Nora van den Puttelaar-van Hal, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2019
Amniotic band sequence in paternal half-siblings with vascular Ehlers-Danlos syndrome
Mary B Callaghan, Rob Hadden, Jon S King, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2012
Clinical utility gene card for: osteogenesis imperfecta
Fleur S van Dijk, Raymond Dalgleish, Fransiska Malfait, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 24, 2012
[Osteogenesis imperfecta: clinical and genetic heterogeneity]
Fleur S van Dijk, Jan M Cobben, Alessandra Maugeri, et al.
Page
of 6