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Human Molecular Genetics
|
July 13, 2001
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus
J L Michaud, F Boucher, A Melnyk, et al.
Revue Des Maladies Respiratoires
|
December 28, 1999
[Surgical treatment of pulmonary metastases of colorectal cancers. 8-year survival and main prognostic factors]
O Baron, A Hamy, J C Roussel, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
November 1, 1988
[Cardiac transplantation at the University Hospital Center of Nantes. 2 years' experience]
T Petit, M Train, M Treilhaud, et al.
Bulletin Du Cancer
|
February 1, 1994
[Well-differentiated papillary mesothelioma of the peritoneum: an attenuated malignant tumor. Review of the literature apropos of a case]
S Bouvier, O Baron, F Nomballais, et al.
Human Genetics
|
December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13
G B Collin, J D Marshall, C F Boerkoel, et al.
Clinical Genetics
|
May 2, 2015
A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly
M Srour, F F Hamdan, Z Gan-Or, et al.
Presse Medicale (Paris, France : 1983)
|
February 7, 1998
[Thymic and bronchial neuroendocrine tumors in multiple endocrine neoplasia type 1. GENEM1]
A Murat, M F Heymann, S Bernat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 1, 1996
[Heart-lung transplantation and cystic fibrosis. Indications and results]
A Haloun, P Despins, D Horeau, et al.
European Journal of Neurology
|
November 8, 2018
MYOD1 involvement in myopathy
F Lopes, M Miguet, B E Mucha, et al.
Clinical Genetics
|
March 19, 2013
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
D Amrom, I Tanyalçin, H Verhelst, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 107) with videos related to
Sort By:
Page
of 11
Human Molecular Genetics
|
July 13, 2001
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus
J L Michaud, F Boucher, A Melnyk, et al.
Revue Des Maladies Respiratoires
|
December 28, 1999
[Surgical treatment of pulmonary metastases of colorectal cancers. 8-year survival and main prognostic factors]
O Baron, A Hamy, J C Roussel, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
November 1, 1988
[Cardiac transplantation at the University Hospital Center of Nantes. 2 years' experience]
T Petit, M Train, M Treilhaud, et al.
Bulletin Du Cancer
|
February 1, 1994
[Well-differentiated papillary mesothelioma of the peritoneum: an attenuated malignant tumor. Review of the literature apropos of a case]
S Bouvier, O Baron, F Nomballais, et al.
Human Genetics
|
December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13
G B Collin, J D Marshall, C F Boerkoel, et al.
Clinical Genetics
|
May 2, 2015
A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly
M Srour, F F Hamdan, Z Gan-Or, et al.
Presse Medicale (Paris, France : 1983)
|
February 7, 1998
[Thymic and bronchial neuroendocrine tumors in multiple endocrine neoplasia type 1. GENEM1]
A Murat, M F Heymann, S Bernat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 1, 1996
[Heart-lung transplantation and cystic fibrosis. Indications and results]
A Haloun, P Despins, D Horeau, et al.
European Journal of Neurology
|
November 8, 2018
MYOD1 involvement in myopathy
F Lopes, M Miguet, B E Mucha, et al.
Clinical Genetics
|
March 19, 2013
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
D Amrom, I Tanyalçin, H Verhelst, et al.
Page
of 11