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Journal of Medical Genetics
|
August 28, 1999
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes
A David, P Bitoun, D Lacombe, et al.
European Journal of Ophthalmology
|
July 9, 2008
Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutation
S Samimi, C Antignac, C Combe, et al.
Archives Francaises De Pediatrie
|
November 1, 1991
[Loperamide and acute diarrhea in infants]
T Lamireau, M Fayon, A Rigot, et al.
European Journal of Cancer (Oxford, England : 1990)
|
February 23, 2002
The EORTC and drug development. European Organisation for Research and Treatment of Cancer
D Lacombe, P Fumoleau, H Zwierzina, et al.
Annales De Genetique
|
January 1, 1997
18p monosomy with midline defects and a de novo satellite identified by FISH
L Taine, C Goizet, Z Q Wen, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes
D Lacombe, P Bioulac-Sage, M Sibout, et al.
Clinical Genetics
|
June 16, 2017
Further delineation of the phenotype caused by biallelic variants in the WDR4 gene
A Trimouille, E Lasseaux, P Barat, et al.
Cancer Treatment Reviews
|
December 1, 2009
EORTC Elderly Task Force experts' opinion for the treatment of colon cancer in older patients
A G Pallis, D Papamichael, R Audisio, et al.
European Journal of Pediatrics
|
February 9, 2000
Costello syndrome: report of six patients including one with an embryonal rhabdomyosarcoma
S Sigaudy, G Vittu, A David, et al.
European Journal of Cancer (Oxford, England : 1990)
|
September 24, 2008
An EORTC phase I study of Bortezomib in combination with oxaliplatin, leucovorin and 5-fluorouracil in patients with advanced colorectal cancer
F Caponigro, D Lacombe, C Twelves, et al.
Page
of 23
Search research articles
Search
Showing results (101-110 of 225) with videos related to
Sort By:
Page
of 23
Journal of Medical Genetics
|
August 28, 1999
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes
A David, P Bitoun, D Lacombe, et al.
European Journal of Ophthalmology
|
July 9, 2008
Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutation
S Samimi, C Antignac, C Combe, et al.
Archives Francaises De Pediatrie
|
November 1, 1991
[Loperamide and acute diarrhea in infants]
T Lamireau, M Fayon, A Rigot, et al.
European Journal of Cancer (Oxford, England : 1990)
|
February 23, 2002
The EORTC and drug development. European Organisation for Research and Treatment of Cancer
D Lacombe, P Fumoleau, H Zwierzina, et al.
Annales De Genetique
|
January 1, 1997
18p monosomy with midline defects and a de novo satellite identified by FISH
L Taine, C Goizet, Z Q Wen, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes
D Lacombe, P Bioulac-Sage, M Sibout, et al.
Clinical Genetics
|
June 16, 2017
Further delineation of the phenotype caused by biallelic variants in the WDR4 gene
A Trimouille, E Lasseaux, P Barat, et al.
Cancer Treatment Reviews
|
December 1, 2009
EORTC Elderly Task Force experts' opinion for the treatment of colon cancer in older patients
A G Pallis, D Papamichael, R Audisio, et al.
European Journal of Pediatrics
|
February 9, 2000
Costello syndrome: report of six patients including one with an embryonal rhabdomyosarcoma
S Sigaudy, G Vittu, A David, et al.
European Journal of Cancer (Oxford, England : 1990)
|
September 24, 2008
An EORTC phase I study of Bortezomib in combination with oxaliplatin, leucovorin and 5-fluorouracil in patients with advanced colorectal cancer
F Caponigro, D Lacombe, C Twelves, et al.
Page
of 23