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H V Firth

Showing results (1-10 of 12) with videos related to

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Journal of Medical Genetics|January 1, 1992
UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disordersH V Firth, R H Lindenbaum
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2021
Systematic assessment of outcomes following a genetic diagnosis identified through a large-scale research study into developmental disordersH Copeland, E Kivuva, H V Firth, et al.
Clinical Genetics|September 15, 2016
Baraitser-Winter cerebrofrontofacial syndromeT M Yates, C L Turner, H V Firth, et al.
Lancet (London, England)|March 30, 1991
Severe limb abnormalities after chorion villus sampling at 56-66 days' gestationH V Firth, P A Boyd, P Chamberlain, et al.
Lancet (London, England)|July 6, 1991
Limb abnormalities and chorion villus samplingH V Firth, P A Boyd, P Chamberlain, et al.
Lancet (London, England)|April 30, 1994
Analysis of limb reduction defects in babies exposed to chorionic villus samplingH V Firth, P A Boyd, P F Chamberlain, et al.
Clinical and Experimental Dermatology|August 21, 2021
Infantile-onset osteoma cutis with pseudopseudohypoparathyroidismN Stembridge, A Durack, J K Gass, et al.
Nature Communications|September 27, 2022
Author Correction: Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing dataC F Wright, E Prigmore, D Rajan, et al.
Nature Communications|July 7, 2019
Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing dataC F Wright, E Prigmore, D Rajan, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|January 1, 1992
UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disordersH V Firth, R H Lindenbaum
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2021
Systematic assessment of outcomes following a genetic diagnosis identified through a large-scale research study into developmental disordersH Copeland, E Kivuva, H V Firth, et al.
Clinical Genetics|September 15, 2016
Baraitser-Winter cerebrofrontofacial syndromeT M Yates, C L Turner, H V Firth, et al.
Lancet (London, England)|March 30, 1991
Severe limb abnormalities after chorion villus sampling at 56-66 days' gestationH V Firth, P A Boyd, P Chamberlain, et al.
Lancet (London, England)|July 6, 1991
Limb abnormalities and chorion villus samplingH V Firth, P A Boyd, P Chamberlain, et al.
Lancet (London, England)|April 30, 1994
Analysis of limb reduction defects in babies exposed to chorionic villus samplingH V Firth, P A Boyd, P F Chamberlain, et al.
Clinical and Experimental Dermatology|August 21, 2021
Infantile-onset osteoma cutis with pseudopseudohypoparathyroidismN Stembridge, A Durack, J K Gass, et al.
Nature Communications|September 27, 2022
Author Correction: Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing dataC F Wright, E Prigmore, D Rajan, et al.
Nature Communications|July 7, 2019
Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing dataC F Wright, E Prigmore, D Rajan, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Pageof 2