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H Plauchu

Showing results (31-40 of 116) with videos related to

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American Journal of Medical Genetics|January 1, 1988
A new acro-cranio-facial dysostosis syndrome in sistersP Kaplan, H Plauchu, N Fitch, et al.
La Revue Du Praticien|October 22, 1998
[Hemophilia. Diagnosis, genetics, complications]C Négrier, C Vinciguerra, S Pinson, et al.
Revue Medicale De Liege|May 15, 1984
[Neonatal screening for Duchenne muscular dystrophy. The Lyons experience]H Plauchu, C Dellamonica, J Cotte, et al.
Journal De Genetique Humaine|December 1, 1980
Duchenne muscular dystrophy: systematic neonatal screening and earlier detection of carriersH Plauchu, C Dellamonica, J Cotte, et al.
Pediatrie|September 1, 1981
[Familial infradiaphragmatic total anomalous pulmonary venous return]J F Blanc, R Bouvier, H Plauchu, et al.
Journal De Genetique Humaine|December 1, 1981
[Meckel syndrome. Difficulties in prenatal diagnosis caused by variability of expression (observations on two families)]H Plauchu, I Kemlin, R Bouvier, et al.
Annales De Biologie Clinique|January 1, 1978
[Hereditary bisalbuminemia. Study of a new familial case in France (author's transl)]A Beaudonnet, J Pichot, H Plauchu, et al.
Annales D'Endocrinologie|November 1, 1975
[Proceedings: Frequency of antigonadotropins antibodies in central hypogonadisms (author's transl)]B Claustrat, L David, H Plauchu, et al.
La Nouvelle Presse Medicale|June 28, 1980
[Antenatal detection of congenital adrenal hyperplasia. Deficiency of 21-hydroxylase]D Floret, H Plauchu, F Berlin, et al.
Pediatrie|March 1, 1980
[Synthetic LHRH hypothalamic hormone test in healthy children from birth to adulthood. Reference values]H Plauchu, B Claustrat, B Betend, et al.
Pageof 12

Showing results (31-40 of 116) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|January 1, 1988
A new acro-cranio-facial dysostosis syndrome in sistersP Kaplan, H Plauchu, N Fitch, et al.
La Revue Du Praticien|October 22, 1998
[Hemophilia. Diagnosis, genetics, complications]C Négrier, C Vinciguerra, S Pinson, et al.
Revue Medicale De Liege|May 15, 1984
[Neonatal screening for Duchenne muscular dystrophy. The Lyons experience]H Plauchu, C Dellamonica, J Cotte, et al.
Journal De Genetique Humaine|December 1, 1980
Duchenne muscular dystrophy: systematic neonatal screening and earlier detection of carriersH Plauchu, C Dellamonica, J Cotte, et al.
Pediatrie|September 1, 1981
[Familial infradiaphragmatic total anomalous pulmonary venous return]J F Blanc, R Bouvier, H Plauchu, et al.
Journal De Genetique Humaine|December 1, 1981
[Meckel syndrome. Difficulties in prenatal diagnosis caused by variability of expression (observations on two families)]H Plauchu, I Kemlin, R Bouvier, et al.
Annales De Biologie Clinique|January 1, 1978
[Hereditary bisalbuminemia. Study of a new familial case in France (author's transl)]A Beaudonnet, J Pichot, H Plauchu, et al.
Annales D'Endocrinologie|November 1, 1975
[Proceedings: Frequency of antigonadotropins antibodies in central hypogonadisms (author's transl)]B Claustrat, L David, H Plauchu, et al.
La Nouvelle Presse Medicale|June 28, 1980
[Antenatal detection of congenital adrenal hyperplasia. Deficiency of 21-hydroxylase]D Floret, H Plauchu, F Berlin, et al.
Pediatrie|March 1, 1980
[Synthetic LHRH hypothalamic hormone test in healthy children from birth to adulthood. Reference values]H Plauchu, B Claustrat, B Betend, et al.
Pageof 12