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Human Genetics
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October 1, 1996
Molecular mapping of a Yq deletion in a patient with normal stature
R Rousseaux-Prévost, J M Rigot, B Delobel, et al.
Clinical Genetics
|
January 6, 2011
Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome
F Petit, M Holder-Espinasse, B Duban-Bedu, et al.
Molecular Human Reproduction
|
September 28, 2004
Chromosome aneuploidy in the spermatozoa of two men with globozoospermia
F Morel, N Douet-Guilbert, A Moerman, et al.
American Journal of Human Genetics
|
July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region
Z Chettouh, M F Croquette, B Delobel, et al.
Human Reproduction (Oxford, England)
|
August 10, 2004
Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: case report
F Morel, N Douet-Guilbert, M-J Le Bris, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome
A Cano, C Rouzier, S Monnot, et al.
Clinical Genetics
|
October 2, 2009
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature
C Nemos, L Lambert, F Giuliano, et al.
The Journal of Pediatrics
|
July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome
H De Leersnyder, M C De Blois, B Claustrat, et al.
International Journal of Radiation Oncology, Biology, Physics
|
July 19, 2014
Random forests to predict rectal toxicity following prostate cancer radiation therapy
Juan D Ospina, Jian Zhu, Ciprian Chira, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]
M Cossée, C Moutou, V Biancalana, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 41) with videos related to
Sort By:
Page
of 5
Human Genetics
|
October 1, 1996
Molecular mapping of a Yq deletion in a patient with normal stature
R Rousseaux-Prévost, J M Rigot, B Delobel, et al.
Clinical Genetics
|
January 6, 2011
Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome
F Petit, M Holder-Espinasse, B Duban-Bedu, et al.
Molecular Human Reproduction
|
September 28, 2004
Chromosome aneuploidy in the spermatozoa of two men with globozoospermia
F Morel, N Douet-Guilbert, A Moerman, et al.
American Journal of Human Genetics
|
July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region
Z Chettouh, M F Croquette, B Delobel, et al.
Human Reproduction (Oxford, England)
|
August 10, 2004
Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: case report
F Morel, N Douet-Guilbert, M-J Le Bris, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome
A Cano, C Rouzier, S Monnot, et al.
Clinical Genetics
|
October 2, 2009
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature
C Nemos, L Lambert, F Giuliano, et al.
The Journal of Pediatrics
|
July 11, 2001
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome
H De Leersnyder, M C De Blois, B Claustrat, et al.
International Journal of Radiation Oncology, Biology, Physics
|
July 19, 2014
Random forests to predict rectal toxicity following prostate cancer radiation therapy
Juan D Ospina, Jian Zhu, Ciprian Chira, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]
M Cossée, C Moutou, V Biancalana, et al.
Page
of 5