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Showing results (91-100 of 9,193) with videos related to
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Clinical Genetics
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June 2, 2016
Expanding the clinical picture of the MECP2 Duplication syndrome
Z Lim, J Downs, K Wong, et al.
Clinical Genetics
|
June 4, 2016
The homozygous R504C mutation in MTO1 gene is responsible for ONCE syndrome
M Á Martín, M T García-Silva, G Barcia, et al.
Clinical Genetics
|
April 11, 2016
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia
J Thevenon, L Duplomb, S Phadke, et al.
Clinical Genetics
|
April 12, 2016
National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendations
M M Sirdah, M S Al-Kahlout, N S Reading
Clinical Genetics
|
November 1, 1989
Impact of public health on human genetics
B Modell, A M Kuliev
Clinical Genetics
|
November 1, 1989
Prospects for cancer control and prevention through genetics
J J Mulvihill
Clinical Genetics
|
November 1, 1989
Autosomal dominant polycystic kidney disease in the 1980's
O Z Dalgaard, S Nørby
Clinical Genetics
|
November 1, 1989
The prevention and management of autosomal recessive conditions. Main example: alpha 1-antitrypsin deficiency
K H Gustavson
Clinical Genetics
|
November 1, 1989
Environmental health hazard handling: statistical and strategic concerns
J Hilden
Clinical Genetics
|
November 1, 1989
Genetic epidemiology of Greenland
B Harvald
Page
of 920
Search research articles
Search
Showing results (91-100 of 9,193) with videos related to
Sort By:
Page
of 920
Clinical Genetics
|
June 2, 2016
Expanding the clinical picture of the MECP2 Duplication syndrome
Z Lim, J Downs, K Wong, et al.
Clinical Genetics
|
June 4, 2016
The homozygous R504C mutation in MTO1 gene is responsible for ONCE syndrome
M Á Martín, M T García-Silva, G Barcia, et al.
Clinical Genetics
|
April 11, 2016
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia
J Thevenon, L Duplomb, S Phadke, et al.
Clinical Genetics
|
April 12, 2016
National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendations
M M Sirdah, M S Al-Kahlout, N S Reading
Clinical Genetics
|
November 1, 1989
Impact of public health on human genetics
B Modell, A M Kuliev
Clinical Genetics
|
November 1, 1989
Prospects for cancer control and prevention through genetics
J J Mulvihill
Clinical Genetics
|
November 1, 1989
Autosomal dominant polycystic kidney disease in the 1980's
O Z Dalgaard, S Nørby
Clinical Genetics
|
November 1, 1989
The prevention and management of autosomal recessive conditions. Main example: alpha 1-antitrypsin deficiency
K H Gustavson
Clinical Genetics
|
November 1, 1989
Environmental health hazard handling: statistical and strategic concerns
J Hilden
Clinical Genetics
|
November 1, 1989
Genetic epidemiology of Greenland
B Harvald
Page
of 920