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European Journal of Medical Genetics
|
December 5, 2006
Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion
M Chaabouni, J Martinovic, D Sanlaville, et al.
Human Genetics
|
May 1, 1988
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11
M Andersson, D C Page, D Pettay, et al.
Annales De Genetique
|
January 1, 1987
The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1
V Blanquet, D Goldgaber, C Turleau, et al.
Humangenetik
|
September 23, 1975
Partial trisomy 9q: a new syndrome
C Turleau, J de Grouchy, F Chavin-Colin, et al.
Human Genetics
|
August 14, 2001
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation
M Rio, C Ozilou, V Cormier-Daire, et al.
Annals of Human Genetics
|
July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32
I Henry, P Gallano, C Besmond, et al.
Cancer Genetics and Cytogenetics
|
April 15, 1985
Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients
C Turleau, J de Grouchy, F Chavin-Colin, et al.
American Journal of Medical Genetics
|
March 1, 1989
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies
C Turleau, M O Cabanis, D Girault, et al.
Human Genetics
|
August 1, 1987
Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism
N Créau-Goldberg, A Gegonne, J Delabar, et al.
American Journal of Medical Genetics
|
April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
L Faivre, G Viot, M Prieur, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 155) with videos related to
Sort By:
Page
of 16
European Journal of Medical Genetics
|
December 5, 2006
Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion
M Chaabouni, J Martinovic, D Sanlaville, et al.
Human Genetics
|
May 1, 1988
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11
M Andersson, D C Page, D Pettay, et al.
Annales De Genetique
|
January 1, 1987
The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1
V Blanquet, D Goldgaber, C Turleau, et al.
Humangenetik
|
September 23, 1975
Partial trisomy 9q: a new syndrome
C Turleau, J de Grouchy, F Chavin-Colin, et al.
Human Genetics
|
August 14, 2001
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation
M Rio, C Ozilou, V Cormier-Daire, et al.
Annals of Human Genetics
|
July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32
I Henry, P Gallano, C Besmond, et al.
Cancer Genetics and Cytogenetics
|
April 15, 1985
Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients
C Turleau, J de Grouchy, F Chavin-Colin, et al.
American Journal of Medical Genetics
|
March 1, 1989
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies
C Turleau, M O Cabanis, D Girault, et al.
Human Genetics
|
August 1, 1987
Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism
N Créau-Goldberg, A Gegonne, J Delabar, et al.
American Journal of Medical Genetics
|
April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
L Faivre, G Viot, M Prieur, et al.
Page
of 16