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Prenatal Diagnosis
|
November 14, 2024
Fetal Presentation of MYRF-Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis
Maud Favier, Elise Brischoux-Boucher, Louise C Pyle, et al.
European Journal of Medical Genetics
|
January 18, 2015
15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients
Clémence Vanlerberghe, Florence Petit, Valérie Malan, et al.
Molecular Syndromology
|
November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign
L Desmyter, M Ghassibe, N Revencu, et al.
Human Mutation
|
January 29, 2014
Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients
Daphné Lehalle, Christopher T Gordon, Myriam Oufadem, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
April 23, 2013
Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature
Edouard Cottereau, Isabelle Mortemousque, Marie-Pierre Moizard, et al.
Clinical Genetics
|
March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases
S Baer, A Afenjar, T Smol, et al.
Journal of Medical Genetics
|
January 26, 2017
<i>STAG1</i> mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability
Daphné Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, et al.
Prenatal Diagnosis
|
August 13, 2024
Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders
Christel Thauvin-Robinet, Aurore Garde, Julian Delanne, et al.
American Journal of Human Genetics
|
December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome
Dagmar Wieczorek, William G Newman, Thomas Wieland, et al.
Clinical Genetics
|
February 16, 2022
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
Bertrand Chesneau, Marion Aubert-Mucca, Félix Fremont, et al.
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of 24
Search research articles
Search
Showing results (201-210 of 232) with videos related to
Sort By:
Page
of 24
Prenatal Diagnosis
|
November 14, 2024
Fetal Presentation of MYRF-Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis
Maud Favier, Elise Brischoux-Boucher, Louise C Pyle, et al.
European Journal of Medical Genetics
|
January 18, 2015
15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients
Clémence Vanlerberghe, Florence Petit, Valérie Malan, et al.
Molecular Syndromology
|
November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign
L Desmyter, M Ghassibe, N Revencu, et al.
Human Mutation
|
January 29, 2014
Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients
Daphné Lehalle, Christopher T Gordon, Myriam Oufadem, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
April 23, 2013
Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature
Edouard Cottereau, Isabelle Mortemousque, Marie-Pierre Moizard, et al.
Clinical Genetics
|
March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases
S Baer, A Afenjar, T Smol, et al.
Journal of Medical Genetics
|
January 26, 2017
<i>STAG1</i> mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability
Daphné Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, et al.
Prenatal Diagnosis
|
August 13, 2024
Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders
Christel Thauvin-Robinet, Aurore Garde, Julian Delanne, et al.
American Journal of Human Genetics
|
December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome
Dagmar Wieczorek, William G Newman, Thomas Wieland, et al.
Clinical Genetics
|
February 16, 2022
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
Bertrand Chesneau, Marion Aubert-Mucca, Félix Fremont, et al.
Page
of 24