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American Journal of Medical Genetics
|
January 1, 1988
A new acro-cranio-facial dysostosis syndrome in sisters
P 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 carriers
H 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.
Page
of 12
Search research articles
Search
Showing results (31-40 of 116) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics
|
January 1, 1988
A new acro-cranio-facial dysostosis syndrome in sisters
P 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 carriers
H 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.
Page
of 12