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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 8, 2001
[Craniofacial development: morphogenesis and determinism]
T Attié-Bitach, M Vekemans, F Encha-Razavi
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 24, 2003
[Molecular diagnosis for the most frequent aneuploïdies with quantitative fluorescent PCR]
D Germanaud, S Audollent, J Augé, et al.
Genomics
|
February 13, 2001
Identification and characterization of an inner ear-expressed human melanoma inhibitory activity (MIA)-like gene (MIAL) with a frequent polymorphism that abolishes translation
N D Rendtorff, M Frödin, T Attié-Bitach, et al.
Human Molecular Genetics
|
June 22, 2000
Expression of the PTEN tumour suppressor protein during human development
O Gimm, T Attié-Bitach, J A Lees, et al.
Advances in Nephrology From the Necker Hospital
|
November 24, 1999
Pax2 in the development of renal and urinary tract diseases
D Joly, R Salomon, J Amiel, et al.
Gene Expression Patterns : GEP
|
November 30, 2004
Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development
M-L Sobrier, T Attié-Bitach, I Netchine, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
MOLAR TOOTH SIGN AND ACROCALLOSAL SYNDROME--A REPORT ON A POLISH FAMILY AND REVIEW OF KIF7 SYNDROMOLOGY
M Krajewska-Walasek, M Kugaudo, M Jędrzejowska, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
P Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
American Journal of Medical Genetics. Part A
|
February 26, 2005
Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation
N Philip, L Colleaux, S Sigaudy, et al.
Hepatology (Baltimore, Md.)
|
August 29, 2000
JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome
C Crosnier, T Attié-Bitach, F Encha-Razavi, et al.
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Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 8, 2001
[Craniofacial development: morphogenesis and determinism]
T Attié-Bitach, M Vekemans, F Encha-Razavi
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 24, 2003
[Molecular diagnosis for the most frequent aneuploïdies with quantitative fluorescent PCR]
D Germanaud, S Audollent, J Augé, et al.
Genomics
|
February 13, 2001
Identification and characterization of an inner ear-expressed human melanoma inhibitory activity (MIA)-like gene (MIAL) with a frequent polymorphism that abolishes translation
N D Rendtorff, M Frödin, T Attié-Bitach, et al.
Human Molecular Genetics
|
June 22, 2000
Expression of the PTEN tumour suppressor protein during human development
O Gimm, T Attié-Bitach, J A Lees, et al.
Advances in Nephrology From the Necker Hospital
|
November 24, 1999
Pax2 in the development of renal and urinary tract diseases
D Joly, R Salomon, J Amiel, et al.
Gene Expression Patterns : GEP
|
November 30, 2004
Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development
M-L Sobrier, T Attié-Bitach, I Netchine, et al.
Genetic Counseling (Geneva, Switzerland)
|
September 10, 2015
MOLAR TOOTH SIGN AND ACROCALLOSAL SYNDROME--A REPORT ON A POLISH FAMILY AND REVIEW OF KIF7 SYNDROMOLOGY
M Krajewska-Walasek, M Kugaudo, M Jędrzejowska, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
P Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
American Journal of Medical Genetics. Part A
|
February 26, 2005
Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation
N Philip, L Colleaux, S Sigaudy, et al.
Hepatology (Baltimore, Md.)
|
August 29, 2000
JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome
C Crosnier, T Attié-Bitach, F Encha-Razavi, et al.
Page
of 3