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European Journal of Human Genetics : EJHG
|
June 13, 2018
Uniparental isodisomy as a cause of recessive Mendelian disease: a diagnostic pitfall with a quick and easy solution in medium/large NGS analyses
Florian Erger, Karin Burau, Michael Elsässer, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2012
A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype
Christina Evers, Johannes W G Janssen, Anna Jauch, et al.
Molecular Ecology
|
November 17, 2006
A chloroplast genealogy of myrmecophytic Macaranga species (Euphorbiaceae) in Southeast Asia reveals hybridization, vicariance and long-distance dispersals
Gudrun Bänfer, Ute Moog, Brigitte Fiala, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Milena Paneque, Clara Serra Juhé, Bela Melegh, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Milena Paneque, Clara Serra Juhé, Bela Melegh, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2014
Oculoectodermal syndrome: report of a new case with a broad clinical spectrum
Deniz Aslan, Rustu Fikret Akata, Julia Schröder, et al.
European Journal of Human Genetics : EJHG
|
July 3, 2025
European training requirements for the specialty of medical genetics
Ute Moog, Jonathan Berg, Siobhan Kerr, et al.
European Journal of Human Genetics : EJHG
|
March 14, 2022
The need for recognition of core professional groups in genetics healthcare services in Europe
Milena Paneque, Thomas Liehr, Clara Serra Juhé, et al.
European Journal of Pediatric Surgery Reports
|
December 27, 2016
Neonatal Gardner Fibroma Leads to Detection of Familial Adenomatous Polyposis: Two Case Reports
Mattias Schäfer, Martina Kadmon, Wolfgang Schmidt, et al.
Journal of Applied Research in Intellectual Disabilities : JARID
|
April 16, 2019
What do parents expect from a genetic diagnosis of their child with intellectual disability?
Nicola Dikow, Ute Moog, Stephanie Karch, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 79) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
June 13, 2018
Uniparental isodisomy as a cause of recessive Mendelian disease: a diagnostic pitfall with a quick and easy solution in medium/large NGS analyses
Florian Erger, Karin Burau, Michael Elsässer, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2012
A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype
Christina Evers, Johannes W G Janssen, Anna Jauch, et al.
Molecular Ecology
|
November 17, 2006
A chloroplast genealogy of myrmecophytic Macaranga species (Euphorbiaceae) in Southeast Asia reveals hybridization, vicariance and long-distance dispersals
Gudrun Bänfer, Ute Moog, Brigitte Fiala, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Milena Paneque, Clara Serra Juhé, Bela Melegh, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Milena Paneque, Clara Serra Juhé, Bela Melegh, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2014
Oculoectodermal syndrome: report of a new case with a broad clinical spectrum
Deniz Aslan, Rustu Fikret Akata, Julia Schröder, et al.
European Journal of Human Genetics : EJHG
|
July 3, 2025
European training requirements for the specialty of medical genetics
Ute Moog, Jonathan Berg, Siobhan Kerr, et al.
European Journal of Human Genetics : EJHG
|
March 14, 2022
The need for recognition of core professional groups in genetics healthcare services in Europe
Milena Paneque, Thomas Liehr, Clara Serra Juhé, et al.
European Journal of Pediatric Surgery Reports
|
December 27, 2016
Neonatal Gardner Fibroma Leads to Detection of Familial Adenomatous Polyposis: Two Case Reports
Mattias Schäfer, Martina Kadmon, Wolfgang Schmidt, et al.
Journal of Applied Research in Intellectual Disabilities : JARID
|
April 16, 2019
What do parents expect from a genetic diagnosis of their child with intellectual disability?
Nicola Dikow, Ute Moog, Stephanie Karch, et al.
Page
of 8