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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 1, 1996
[Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients]
A Levy-Mozziconacci, D Lacombe, B Leheup, et al.
Journal of Human Genetics
|
August 11, 2006
Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization
C Bonnet, M J Grégoire, K Brochet, et al.
Clinical Genetics
|
March 18, 2004
Terminal deletion of the long arm of chromosome 10
S Scigliano, M J Grégoire, M Schmitt, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 3, 2017
[22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis]
T Ingrao, L Lambert, M Valduga, et al.
Gynecologie, Obstetrique & Fertilite
|
March 19, 2013
[Azoospermia and 45,X/46,XY chromosomal mosaicism: a case report]
M Le Chatton, A Zaccabri, M Agopiantz, et al.
The Biochemical Journal
|
August 15, 1992
Intrinsic factor receptor during fetal development of the human intestine
H Schohn, J L Guéant, B Leheup, et al.
Molecular Genetics and Metabolism
|
September 21, 2013
Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?
A Wiedemann, B Leheup, S-F Battaglia-Hsu, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 28, 2019
Hypotrichosis with keratosis follicular and hyperostosis: a new phenotype due to GJA1 mutation
A C Bursztejn, C Magdelaine, B Mortemousque, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardation
C Bonnet, B Leheup, M Béri, et al.
Journal of Human Genetics
|
July 25, 2008
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene
C Bonnet, M-J Grégoire, M Vibert, et al.
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of 9
Search research articles
Search
Showing results (31-40 of 82) with videos related to
Sort By:
Page
of 9
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 1, 1996
[Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients]
A Levy-Mozziconacci, D Lacombe, B Leheup, et al.
Journal of Human Genetics
|
August 11, 2006
Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization
C Bonnet, M J Grégoire, K Brochet, et al.
Clinical Genetics
|
March 18, 2004
Terminal deletion of the long arm of chromosome 10
S Scigliano, M J Grégoire, M Schmitt, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 3, 2017
[22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis]
T Ingrao, L Lambert, M Valduga, et al.
Gynecologie, Obstetrique & Fertilite
|
March 19, 2013
[Azoospermia and 45,X/46,XY chromosomal mosaicism: a case report]
M Le Chatton, A Zaccabri, M Agopiantz, et al.
The Biochemical Journal
|
August 15, 1992
Intrinsic factor receptor during fetal development of the human intestine
H Schohn, J L Guéant, B Leheup, et al.
Molecular Genetics and Metabolism
|
September 21, 2013
Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?
A Wiedemann, B Leheup, S-F Battaglia-Hsu, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 28, 2019
Hypotrichosis with keratosis follicular and hyperostosis: a new phenotype due to GJA1 mutation
A C Bursztejn, C Magdelaine, B Mortemousque, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardation
C Bonnet, B Leheup, M Béri, et al.
Journal of Human Genetics
|
July 25, 2008
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene
C Bonnet, M-J Grégoire, M Vibert, et al.
Page
of 9