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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Ronja Hollstein, Nina Ishorst, Annette Lischka, et al.
Pediatric Dermatology
|
September 11, 2013
Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene
Arti Nanda, Sandra M Pasternack, Hassnaa Mahmoudi, et al.
Scientific Reports
|
October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formation
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
HGG Advances
|
January 2, 2023
Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of <i>de novo</i> mutations
Hanna K Zieger, Leonie Weinhold, Axel Schmidt, et al.
Human Molecular Genetics
|
June 21, 2026
Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix
Julia A Capecki, Helena Shkuro, Öznur Yilmaz, et al.
HGG Advances
|
January 20, 2022
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate
Julia Welzenbach, Nigel L Hammond, Miloš Nikolić, et al.
Human Molecular Genetics
|
January 15, 2017
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only
Kerstin U Ludwig, Anne C Böhmer, John Bowes, et al.
Genes
|
December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility Gene
Iris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Birth Defects Research
|
March 3, 2018
Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample
Nina Ishorst, Paola Francheschelli, Anne C Böhmer, et al.
Human Mutation
|
May 18, 2021
Extending the allelic spectrum at noncoding risk loci of orofacial clefting
Frederic Thieme, Leonie Henschel, Nigel L Hammond, et al.
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Search research articles
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Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Ronja Hollstein, Nina Ishorst, Annette Lischka, et al.
Pediatric Dermatology
|
September 11, 2013
Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene
Arti Nanda, Sandra M Pasternack, Hassnaa Mahmoudi, et al.
Scientific Reports
|
October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formation
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
HGG Advances
|
January 2, 2023
Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of <i>de novo</i> mutations
Hanna K Zieger, Leonie Weinhold, Axel Schmidt, et al.
Human Molecular Genetics
|
June 21, 2026
Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix
Julia A Capecki, Helena Shkuro, Öznur Yilmaz, et al.
HGG Advances
|
January 20, 2022
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate
Julia Welzenbach, Nigel L Hammond, Miloš Nikolić, et al.
Human Molecular Genetics
|
January 15, 2017
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only
Kerstin U Ludwig, Anne C Böhmer, John Bowes, et al.
Genes
|
December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility Gene
Iris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Birth Defects Research
|
March 3, 2018
Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample
Nina Ishorst, Paola Francheschelli, Anne C Böhmer, et al.
Human Mutation
|
May 18, 2021
Extending the allelic spectrum at noncoding risk loci of orofacial clefting
Frederic Thieme, Leonie Henschel, Nigel L Hammond, et al.
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of 2