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American Journal of Medical Genetics
|
January 30, 1995
Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)
R J Gibbons, L Brueton, V J Buckle, et al.
European Journal of Human Genetics : EJHG
|
August 31, 2001
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis
S Gerber, I Perrault, S Hanein, et al.
Prenatal Diagnosis
|
June 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?
A Gibbs, R Braham, V Ramachandran, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
January 3, 2026
Prenatal presentation of fetal bradycardia and long QT syndrome
S Chivers, V Zidere, T V Vigneswaran, et al.
Journal of Medical Genetics
|
May 8, 2007
Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics
J Barwell, L Pangon, S Hodgson, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 13, 2021
Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis
F Mone, R Y Eberhardt, M E Hurles, et al.
Journal of Medical Genetics
|
March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
B B de Vries, S M White, S J Knight, et al.
Human Molecular Genetics
|
August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome
M Kalff-Suske, A Wild, J Topp, et al.
American Journal of Human Genetics
|
April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene
D M Hagan, A J Ross, T Strachan, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 15, 2003
The UK national study of magnetic resonance imaging as a method of screening for breast cancer (MARIBS)
M O Leach, R A Eeles, L W Turnbull, et al.
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Search research articles
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Showing results (21-30 of 30) with videos related to
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Page
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You have reached the last page of results.
This site can display upto 30 results.
American Journal of Medical Genetics
|
January 30, 1995
Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)
R J Gibbons, L Brueton, V J Buckle, et al.
European Journal of Human Genetics : EJHG
|
August 31, 2001
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis
S Gerber, I Perrault, S Hanein, et al.
Prenatal Diagnosis
|
June 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?
A Gibbs, R Braham, V Ramachandran, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
January 3, 2026
Prenatal presentation of fetal bradycardia and long QT syndrome
S Chivers, V Zidere, T V Vigneswaran, et al.
Journal of Medical Genetics
|
May 8, 2007
Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics
J Barwell, L Pangon, S Hodgson, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 13, 2021
Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis
F Mone, R Y Eberhardt, M E Hurles, et al.
Journal of Medical Genetics
|
March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
B B de Vries, S M White, S J Knight, et al.
Human Molecular Genetics
|
August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome
M Kalff-Suske, A Wild, J Topp, et al.
American Journal of Human Genetics
|
April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene
D M Hagan, A J Ross, T Strachan, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 15, 2003
The UK national study of magnetic resonance imaging as a method of screening for breast cancer (MARIBS)
M O Leach, R A Eeles, L W Turnbull, et al.
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of 3