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Archives Francaises De Pediatrie
|
January 1, 1986
[Value of mexiletine in the treatment of Thomsen-Becker myotonia]
B Leheup, F Himon, A Morali, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
July 2, 1998
[Prenatal diagnosis of a pancreatic cyst due to Ivemark II syndrome]
M P Quéméré, P Droullé, B Leheup, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 25, 2015
[Sandifer's syndrome in a 5-month-old child with suspicion of infantile spasms]
M Wirth, C Bonnemains, J Auger, et al.
Journal De Genetique Humaine
|
January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]
P Mujica, B Leheup, S Gilgenkrantz, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 15, 2004
[Grave's disease in children with 22q11 deletion. Report of three cases]
J Gosselin, B Lebon-Labich, H Lucron, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 6, 1998
[Noonan syndrome: an enigma]
J M Limal, D Bonnet, Y L Bouc, et al.
Pediatrie
|
January 1, 1989
[Evaluation of short stature in boys: delayed growth or constitutional short size?]
L Paulin, B Leheup, R Gueguen, et al.
Pediatrie
|
January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]
C Pernot, A M Worms, F Marçon, et al.
Clinical Genetics
|
December 3, 2013
Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome
C Lacoste, B Leheup, I Agouti, et al.
Orthopaedics & Traumatology, Surgery & Research : OTSR
|
September 14, 2014
Radiological and clinical analysis of Madelung's deformity in children
S Huguet, B Leheup, M Aslan, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 82) with videos related to
Sort By:
Page
of 9
Archives Francaises De Pediatrie
|
January 1, 1986
[Value of mexiletine in the treatment of Thomsen-Becker myotonia]
B Leheup, F Himon, A Morali, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
July 2, 1998
[Prenatal diagnosis of a pancreatic cyst due to Ivemark II syndrome]
M P Quéméré, P Droullé, B Leheup, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 25, 2015
[Sandifer's syndrome in a 5-month-old child with suspicion of infantile spasms]
M Wirth, C Bonnemains, J Auger, et al.
Journal De Genetique Humaine
|
January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]
P Mujica, B Leheup, S Gilgenkrantz, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 15, 2004
[Grave's disease in children with 22q11 deletion. Report of three cases]
J Gosselin, B Lebon-Labich, H Lucron, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 6, 1998
[Noonan syndrome: an enigma]
J M Limal, D Bonnet, Y L Bouc, et al.
Pediatrie
|
January 1, 1989
[Evaluation of short stature in boys: delayed growth or constitutional short size?]
L Paulin, B Leheup, R Gueguen, et al.
Pediatrie
|
January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]
C Pernot, A M Worms, F Marçon, et al.
Clinical Genetics
|
December 3, 2013
Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome
C Lacoste, B Leheup, I Agouti, et al.
Orthopaedics & Traumatology, Surgery & Research : OTSR
|
September 14, 2014
Radiological and clinical analysis of Madelung's deformity in children
S Huguet, B Leheup, M Aslan, et al.
Page
of 9