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S M White

Showing results (141-150 of 150) with videos related to

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Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|December 21, 2020
An overall view of temperature oscillations in the solar chromosphere with ALMAS Jafarzadeh, S Wedemeyer, B Fleck, et al.
Clinical Genetics|February 6, 2004
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutationsG Turner, K M Lower, S M White, et al.
Clinical Genetics|February 6, 2013
Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?M J M Nowaczyk, B A Thompson, S Zeesman, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 22, 2013
Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?D Ganesamoorthy, D L Bruno, G McGillivray, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Journal of Medical Genetics|March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklistB B de Vries, S M White, S J Knight, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Anaesthesia|March 7, 2018
International Fragility Fracture Network Delphi consensus statement on the principles of anaesthesia for patients with hip fractureS M White, F Altermatt, J Barry, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Clinical Genetics|October 27, 2015
Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|December 21, 2020
An overall view of temperature oscillations in the solar chromosphere with ALMAS Jafarzadeh, S Wedemeyer, B Fleck, et al.
Clinical Genetics|February 6, 2004
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutationsG Turner, K M Lower, S M White, et al.
Clinical Genetics|February 6, 2013
Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?M J M Nowaczyk, B A Thompson, S Zeesman, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 22, 2013
Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?D Ganesamoorthy, D L Bruno, G McGillivray, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Journal of Medical Genetics|March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklistB B de Vries, S M White, S J Knight, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Anaesthesia|March 7, 2018
International Fragility Fracture Network Delphi consensus statement on the principles of anaesthesia for patients with hip fractureS M White, F Altermatt, J Barry, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Clinical Genetics|October 27, 2015
Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.
Pageof 15