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Journal of Medical Genetics
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November 20, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Prenatal Diagnosis
|
February 2, 2018
Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing
Nathalie Brison, Maria Neofytou, Luc Dehaspe, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2025
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2024
Mapping genes for human face shape: exploration of univariate phenotyping strategies
Meng Yuan, Seppe Goovaerts, Michiel Vanneste, et al.
Plos Computational Biology
|
December 2, 2024
Mapping genes for human face shape: Exploration of univariate phenotyping strategies
Meng Yuan, Seppe Goovaerts, Michiel Vanneste, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 15, 2019
Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening
Nathalie Brison, Jazz Storms, Darine Villela, et al.
Biorxiv : the Preprint Server for Biology
|
December 18, 2023
Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population
Michiel Vanneste, Hanne Hoskens, Seppe Goovaerts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 2, 2016
Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies
Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, et al.
Human Molecular Genetics
|
October 14, 2006
Sesn1 is a novel gene for left-right asymmetry and mediating nodal signaling
Hilde Peeters, Marianne L Voz, Kristin Verschueren, et al.
Journal of Medical Genetics
|
January 15, 2020
The clinical relevance of intragenic <i>NRXN1</i> deletions
Nele Cosemans, Laura Vandenhove, Annick Vogels, et al.
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Search research articles
Search
Showing results (61-70 of 99) with videos related to
Sort By:
Page
of 10
Journal of Medical Genetics
|
November 20, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Prenatal Diagnosis
|
February 2, 2018
Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing
Nathalie Brison, Maria Neofytou, Luc Dehaspe, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2025
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2024
Mapping genes for human face shape: exploration of univariate phenotyping strategies
Meng Yuan, Seppe Goovaerts, Michiel Vanneste, et al.
Plos Computational Biology
|
December 2, 2024
Mapping genes for human face shape: Exploration of univariate phenotyping strategies
Meng Yuan, Seppe Goovaerts, Michiel Vanneste, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 15, 2019
Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening
Nathalie Brison, Jazz Storms, Darine Villela, et al.
Biorxiv : the Preprint Server for Biology
|
December 18, 2023
Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population
Michiel Vanneste, Hanne Hoskens, Seppe Goovaerts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 2, 2016
Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies
Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, et al.
Human Molecular Genetics
|
October 14, 2006
Sesn1 is a novel gene for left-right asymmetry and mediating nodal signaling
Hilde Peeters, Marianne L Voz, Kristin Verschueren, et al.
Journal of Medical Genetics
|
January 15, 2020
The clinical relevance of intragenic <i>NRXN1</i> deletions
Nele Cosemans, Laura Vandenhove, Annick Vogels, et al.
Page
of 10