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American Journal of Medical Genetics. Part A
|
March 26, 2014
Chromosomal rearrangements in patients with clinical features of Silver-Russell syndrome
Siv Fokstuen, Dieter Kotzot
Revue Medicale Suisse
|
May 3, 2023
[Rare causes of Hypophosphatemia: diagnostic approach]
Andrea Trombetti, Siv Fokstuen, Paloma Parvex
Revue Medicale Suisse
|
February 25, 2014
[Antenatal diagnosis: the revolution of new technologies]
Siv Fokstuen, Frédérique Sloan-Béna, Olivier lrion
Child Neurology Open
|
September 4, 2023
Odyssey of a Misclassified Genomic Variant: Insight from an Incidental Finding Assessment
Omar Zgheib, Andrea Trombetti, André Juillerat, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2003
FOXL2-mutations in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES); challenges for genetic counseling in female patients
Siv Fokstuen, Stylianos E Antonarakis, Jean-Louis Blouin
Congenital Anomalies
|
August 24, 2010
Are abdominal wall defects and external genitalia anomalies randomly expressed in some families?
Ambroise Wonkam, Philipe Extermann, Jacques Birraux, et al.
Clinical Genetics
|
January 31, 2025
Toe Polydactyly and Supernumerary Nipple: Broadening the Phenotypic Spectrum of STAR Syndrome
Omar Zgheib, Léa Jacques, Louise Frizon, et al.
Journal of Medical Ethics
|
January 1, 2017
Defining categories of actionability for secondary findings in next-generation sequencing
Celine Moret, Alex Mauron, Siv Fokstuen, et al.
Journal of Clinical Medicine
|
October 14, 2022
Brugada Syndrome Associated with Different Heterozygous <i>SCN5A</i> Variants in Two Unrelated Families
Nadine Molitor, Argelia Medeiros-Domingo, Siv Fokstuen, et al.
Journal of Medical Case Reports
|
December 13, 2019
Management of delivery of a fetus with autosomal recessive polycystic kidney disease: a case report of abdominal dystocia and review of the literature
Sarah Belin, Cristina Delco, Paloma Parvex, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics. Part A
|
March 26, 2014
Chromosomal rearrangements in patients with clinical features of Silver-Russell syndrome
Siv Fokstuen, Dieter Kotzot
Revue Medicale Suisse
|
May 3, 2023
[Rare causes of Hypophosphatemia: diagnostic approach]
Andrea Trombetti, Siv Fokstuen, Paloma Parvex
Revue Medicale Suisse
|
February 25, 2014
[Antenatal diagnosis: the revolution of new technologies]
Siv Fokstuen, Frédérique Sloan-Béna, Olivier lrion
Child Neurology Open
|
September 4, 2023
Odyssey of a Misclassified Genomic Variant: Insight from an Incidental Finding Assessment
Omar Zgheib, Andrea Trombetti, André Juillerat, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2003
FOXL2-mutations in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES); challenges for genetic counseling in female patients
Siv Fokstuen, Stylianos E Antonarakis, Jean-Louis Blouin
Congenital Anomalies
|
August 24, 2010
Are abdominal wall defects and external genitalia anomalies randomly expressed in some families?
Ambroise Wonkam, Philipe Extermann, Jacques Birraux, et al.
Clinical Genetics
|
January 31, 2025
Toe Polydactyly and Supernumerary Nipple: Broadening the Phenotypic Spectrum of STAR Syndrome
Omar Zgheib, Léa Jacques, Louise Frizon, et al.
Journal of Medical Ethics
|
January 1, 2017
Defining categories of actionability for secondary findings in next-generation sequencing
Celine Moret, Alex Mauron, Siv Fokstuen, et al.
Journal of Clinical Medicine
|
October 14, 2022
Brugada Syndrome Associated with Different Heterozygous <i>SCN5A</i> Variants in Two Unrelated Families
Nadine Molitor, Argelia Medeiros-Domingo, Siv Fokstuen, et al.
Journal of Medical Case Reports
|
December 13, 2019
Management of delivery of a fetus with autosomal recessive polycystic kidney disease: a case report of abdominal dystocia and review of the literature
Sarah Belin, Cristina Delco, Paloma Parvex, et al.
Page
of 3