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Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
November 29, 2014
Human Genetics Society of Australasia position statement: population-based carrier screening for cystic fibrosis
Martin B Delatycki, Jo Burke, Louise Christie, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2017
Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy
Lisa J Ewans, Michael Field, Ying Zhu, et al.
Human Genetics
|
March 3, 2007
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
Guy Froyen, Marijke Bauters, Jackie Boyle, et al.
European Journal of Human Genetics : EJHG
|
October 15, 2009
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation
Sinitdhorn Rujirabanjerd, John Nelson, Patrick S Tarpey, et al.
American Journal of Human Genetics
|
May 6, 2008
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation
Florence Molinari, François Foulquier, Patrick S Tarpey, et al.
BMJ Public Health
|
January 17, 2025
Evaluating the effects, implementation experience and political economy of primary healthcare facility autonomy reforms within counties in Kenya: a mixed methods study protocol
Anita Musiega, Beatrice Amboko, Beryl Maritim, et al.
Health Research Policy and Systems
|
January 28, 2025
Evaluating the impact, implementation experience and political economy of primary care networks in Kenya: protocol for a mixed methods study
Beatrice Amboko, Jacinta Nzinga, Benjamin Tsofa, et al.
Wellcome Open Research
|
September 16, 2024
A mixed methods study examining the impact of primary health care financing transitions on facility functioning and service delivery in Kenya: a study protocol
Rose Nabi Deborah Karimi Muthuri, Jacinta Nzinga, Benjamin Tsofa, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
October 13, 2011
Aryl-aryl bond formation by the fluoride-free cross-coupling of aryldisiloxanes with aryl bromides
Christine M Boehner, Elizabeth C Frye, Kieron M G O'Connell, et al.
European Journal of Medical Genetics
|
November 6, 2007
Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH
Ludmila Kousoulidou, Sven Parkel, Olga Zilina, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
November 29, 2014
Human Genetics Society of Australasia position statement: population-based carrier screening for cystic fibrosis
Martin B Delatycki, Jo Burke, Louise Christie, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2017
Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy
Lisa J Ewans, Michael Field, Ying Zhu, et al.
Human Genetics
|
March 3, 2007
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
Guy Froyen, Marijke Bauters, Jackie Boyle, et al.
European Journal of Human Genetics : EJHG
|
October 15, 2009
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation
Sinitdhorn Rujirabanjerd, John Nelson, Patrick S Tarpey, et al.
American Journal of Human Genetics
|
May 6, 2008
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation
Florence Molinari, François Foulquier, Patrick S Tarpey, et al.
BMJ Public Health
|
January 17, 2025
Evaluating the effects, implementation experience and political economy of primary healthcare facility autonomy reforms within counties in Kenya: a mixed methods study protocol
Anita Musiega, Beatrice Amboko, Beryl Maritim, et al.
Health Research Policy and Systems
|
January 28, 2025
Evaluating the impact, implementation experience and political economy of primary care networks in Kenya: protocol for a mixed methods study
Beatrice Amboko, Jacinta Nzinga, Benjamin Tsofa, et al.
Wellcome Open Research
|
September 16, 2024
A mixed methods study examining the impact of primary health care financing transitions on facility functioning and service delivery in Kenya: a study protocol
Rose Nabi Deborah Karimi Muthuri, Jacinta Nzinga, Benjamin Tsofa, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
October 13, 2011
Aryl-aryl bond formation by the fluoride-free cross-coupling of aryldisiloxanes with aryl bromides
Christine M Boehner, Elizabeth C Frye, Kieron M G O'Connell, et al.
European Journal of Medical Genetics
|
November 6, 2007
Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH
Ludmila Kousoulidou, Sven Parkel, Olga Zilina, et al.
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of 6