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J Battin

Showing results (71-80 of 222) with videos related to

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Archives Francaises De Pediatrie|November 1, 1971
[Exostosing disease with voluminous osteochondroma of the scapula]J Battin, X Azanza, J P Héhunstre
Annales De Pediatrie|February 1, 1989
[Acute myelomonocytic leukemia with eosinophils. Apropos of a case with a cytogenetic analysis and nosologic discussion]J Battin, V Guérin-Darmendrail, V Martin
American Journal of Medical Genetics|September 1, 1992
Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3D Lacombe, R Saura, L Taine, et al.
Bulletin De L'Academie Nationale De Medecine|September 16, 2000
[Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype]J Battin, D Lacombe, L Taine, et al.
Bordeaux Medical|October 1, 1970
[Prader-Willi-Labhardt syndrome in a girl with development of an insulinoprivic diabete]J Battin, J Aubertin, J Alberty, et al.
Human Genetics|February 1, 1980
Altered sensitivity to cholchicine and PHA in human cultured cellsY Chamla, M Roumy, M Lassègues, et al.
Journal of Medical Genetics|August 1, 1993
Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromesD Lacombe, F Serville, D Marchand, et al.
Human Genetics|September 22, 1977
Partial 9q trisomy associated with a 9,21 translocationY Chamla, C Bilbeissi, M Micheau, et al.
Archives Francaises De Pediatrie|June 1, 1984
[Pelvic echographic data during normal and pathological development in girls]M Colle, A Calabet, L Cadier, et al.
Pediatrie|March 1, 1974
[Essential familial hyperlipemia type I. Apropos of a case]P Chavoix, F Siriex, R Crockett, et al.
Pageof 23

Showing results (71-80 of 222) with videos related to

Sort By:
Pageof 23
Archives Francaises De Pediatrie|November 1, 1971
[Exostosing disease with voluminous osteochondroma of the scapula]J Battin, X Azanza, J P Héhunstre
Annales De Pediatrie|February 1, 1989
[Acute myelomonocytic leukemia with eosinophils. Apropos of a case with a cytogenetic analysis and nosologic discussion]J Battin, V Guérin-Darmendrail, V Martin
American Journal of Medical Genetics|September 1, 1992
Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3D Lacombe, R Saura, L Taine, et al.
Bulletin De L'Academie Nationale De Medecine|September 16, 2000
[Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype]J Battin, D Lacombe, L Taine, et al.
Bordeaux Medical|October 1, 1970
[Prader-Willi-Labhardt syndrome in a girl with development of an insulinoprivic diabete]J Battin, J Aubertin, J Alberty, et al.
Human Genetics|February 1, 1980
Altered sensitivity to cholchicine and PHA in human cultured cellsY Chamla, M Roumy, M Lassègues, et al.
Journal of Medical Genetics|August 1, 1993
Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromesD Lacombe, F Serville, D Marchand, et al.
Human Genetics|September 22, 1977
Partial 9q trisomy associated with a 9,21 translocationY Chamla, C Bilbeissi, M Micheau, et al.
Archives Francaises De Pediatrie|June 1, 1984
[Pelvic echographic data during normal and pathological development in girls]M Colle, A Calabet, L Cadier, et al.
Pediatrie|March 1, 1974
[Essential familial hyperlipemia type I. Apropos of a case]P Chavoix, F Siriex, R Crockett, et al.
Pageof 23