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P Sarda

Showing results (31-40 of 150) with videos related to

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Journal of Medical Genetics|April 1, 1992
Interstitial deletion of the distal long arm of chromosome 4P Sarda, G Lefort, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Multiple congenital anomalies associated with an oto-palato-digital syndrome type IIP Blanchet, G Lefort, M C Eglin, et al.
Cureus|November 21, 2022
Intra-body Networks and Molecular Communication Networks in Diagnostic SciencesPrayas P Sarda, Sourya Acharya, Shreyash Huse, et al.
Eye, Ear, Nose & Throat Monthly|May 1, 1972
A study of glaucoma in relation with thyroid dysfunctionR P Sarda, A S Mehrotra, R Adnani, et al.
Pediatrie|December 1, 1983
[Streptococcus group B neonatal infection and postnatal diaphragmatic hernia]F Montoya, P Montoya, J F Eliaou, et al.
American Journal of Medical Genetics|February 11, 1997
Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.
Pediatrie|January 1, 1989
[The CHARGE association]C Allouche, P Sarda, F Tronc, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|August 10, 2019
Global incidence of bronchopulmonary dysplasia among extremely preterm infants: a systematic literature reviewCsaba Siffel, Kristin D Kistler, Juliana F M Lewis, et al.
Haematologica|December 29, 1998
The role of serum transferrin receptor in the diagnosis of iron deficiencyA F Remacha, M P Sarda, M Parellada, et al.
European Journal of Clinical Nutrition|January 11, 2000
Alpha linolenic acid in cholesterol esters: a marker of alphalinolenic acid intake in newbornsF Babin, A Rodriguez, P Sarda, et al.
Pageof 15

Showing results (31-40 of 150) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|April 1, 1992
Interstitial deletion of the distal long arm of chromosome 4P Sarda, G Lefort, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Multiple congenital anomalies associated with an oto-palato-digital syndrome type IIP Blanchet, G Lefort, M C Eglin, et al.
Cureus|November 21, 2022
Intra-body Networks and Molecular Communication Networks in Diagnostic SciencesPrayas P Sarda, Sourya Acharya, Shreyash Huse, et al.
Eye, Ear, Nose & Throat Monthly|May 1, 1972
A study of glaucoma in relation with thyroid dysfunctionR P Sarda, A S Mehrotra, R Adnani, et al.
Pediatrie|December 1, 1983
[Streptococcus group B neonatal infection and postnatal diaphragmatic hernia]F Montoya, P Montoya, J F Eliaou, et al.
American Journal of Medical Genetics|February 11, 1997
Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.
Pediatrie|January 1, 1989
[The CHARGE association]C Allouche, P Sarda, F Tronc, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|August 10, 2019
Global incidence of bronchopulmonary dysplasia among extremely preterm infants: a systematic literature reviewCsaba Siffel, Kristin D Kistler, Juliana F M Lewis, et al.
Haematologica|December 29, 1998
The role of serum transferrin receptor in the diagnosis of iron deficiencyA F Remacha, M P Sarda, M Parellada, et al.
European Journal of Clinical Nutrition|January 11, 2000
Alpha linolenic acid in cholesterol esters: a marker of alphalinolenic acid intake in newbornsF Babin, A Rodriguez, P Sarda, et al.
Pageof 15