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H Robin

Showing results (221-230 of 297) with videos related to

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American Journal of Medical Genetics. Part A|February 13, 2009
Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1Kara Goodin, Sandra Prucka, Audie L Woolley, et al.
Clinical and Laboratory Haematology|January 1, 1993
A computerized expert system for handling the output of the Technicon H1 haematology analyserP R Burgess, G W Kershaw, R H Coleman, et al.
The British Journal of Dermatology|August 1, 1997
IgA-epidermolysis bullosa acquisita in a child resulting in blindnessF Caux, G Kirtschig, F Lemarchand-Venencie, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Exhale nitric oxide (NO) and respiratory function measured with body plethysmography in children]L Storme, Y Riou, F Leclerc, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
Trisomy 18: A survey of opinions, attitudes, and practices of neonatologistsAdam P Jacobs, Akila Subramaniam, Ying Tang, et al.
Tropical Life Sciences Research|December 22, 2022
Physicochemical Properties of Honey from Contract Beekeepers, Street Vendors and Branded Honey in Sabah, MalaysiaA H Robin Lim, Lum Mok Sam, Januarius Gobilik, et al.
American Journal of Medical Genetics|November 15, 1994
Non-immune hydrops fetalis associated with impaired fetal movement: a case report and reviewN H Robin, M T Curtis, W Mulla, et al.
The Journal of Pediatrics|March 20, 1998
Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagenD A Sirko-Osadsa, M A Murray, J A Scott, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1977
[Determination of global diffusion of CO2 and its partial components under assisted respiration. Technical problems and practical value in respiratory resuscitation]C Chopin, M C Chambrin, H Robin, et al.
American Journal of Medical Genetics. Part A|September 15, 2018
A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13CJariya Upadia, Patrick R Gonzales, T Prescott Atkinson, et al.
Pageof 30

Showing results (221-230 of 297) with videos related to

Sort By:
Pageof 30
American Journal of Medical Genetics. Part A|February 13, 2009
Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1Kara Goodin, Sandra Prucka, Audie L Woolley, et al.
Clinical and Laboratory Haematology|January 1, 1993
A computerized expert system for handling the output of the Technicon H1 haematology analyserP R Burgess, G W Kershaw, R H Coleman, et al.
The British Journal of Dermatology|August 1, 1997
IgA-epidermolysis bullosa acquisita in a child resulting in blindnessF Caux, G Kirtschig, F Lemarchand-Venencie, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Exhale nitric oxide (NO) and respiratory function measured with body plethysmography in children]L Storme, Y Riou, F Leclerc, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
Trisomy 18: A survey of opinions, attitudes, and practices of neonatologistsAdam P Jacobs, Akila Subramaniam, Ying Tang, et al.
Tropical Life Sciences Research|December 22, 2022
Physicochemical Properties of Honey from Contract Beekeepers, Street Vendors and Branded Honey in Sabah, MalaysiaA H Robin Lim, Lum Mok Sam, Januarius Gobilik, et al.
American Journal of Medical Genetics|November 15, 1994
Non-immune hydrops fetalis associated with impaired fetal movement: a case report and reviewN H Robin, M T Curtis, W Mulla, et al.
The Journal of Pediatrics|March 20, 1998
Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagenD A Sirko-Osadsa, M A Murray, J A Scott, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1977
[Determination of global diffusion of CO2 and its partial components under assisted respiration. Technical problems and practical value in respiratory resuscitation]C Chopin, M C Chambrin, H Robin, et al.
American Journal of Medical Genetics. Part A|September 15, 2018
A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13CJariya Upadia, Patrick R Gonzales, T Prescott Atkinson, et al.
Pageof 30