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Journal of Medical Genetics
|
April 16, 1999
Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q
M F Portnoï, S Boutchneï, F Bouscarat, et al.
Human Reproduction (Oxford, England)
|
June 6, 2006
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients
M F Portnoï, A Aboura, G Tachdjian, et al.
Clinical Genetics
|
September 27, 2000
Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation
M F Portnoï, N Bouayed-Abdelmoula, M Mirc, et al.
Prenatal Diagnosis
|
January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 14 results.
Journal of Medical Genetics
|
April 16, 1999
Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q
M F Portnoï, S Boutchneï, F Bouscarat, et al.
Human Reproduction (Oxford, England)
|
June 6, 2006
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients
M F Portnoï, A Aboura, G Tachdjian, et al.
Clinical Genetics
|
September 27, 2000
Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation
M F Portnoï, N Bouayed-Abdelmoula, M Mirc, et al.
Prenatal Diagnosis
|
January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Page
of 2