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The British Journal of Radiology
|
October 1, 1990
Choroid plexus cysts and chromosomal defects
J G Thorpe-Beeston, C M Gosden, K H Nicolaides
American Journal of Obstetrics and Gynecology
|
February 1, 1993
Fetal growth retardation: associated malformations and chromosomal abnormalities
R J Snijders, C Sherrod, C M Gosden, et al.
American Journal of Human Genetics
|
September 1, 1993
De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier
D T Bonthron, S J Smith, J Fantes, et al.
Fetal Diagnosis and Therapy
|
January 1, 1992
Fetal nuchal oedema: associated malformations and chromosomal defects
K H Nicolaides, G Azar, R J Snijders, et al.
American Journal of Human Genetics
|
February 1, 1994
Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3
L Strain, C M Gosden, D J Brock, et al.
Human Genetics
|
April 1, 1988
Linkage heterogeneity and fragile X
J F Clayton, C M Gosden, N D Hastie, et al.
Clinical Genetics
|
June 1, 1979
Satellite DNA loss and nucleolar organiser activity in an individual with a de novo chromosome 13,14 translocation
J R Gosden, C M Gosden, S S Lawrie, et al.
Prenatal Diagnosis
|
March 1, 1987
Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid
T P Webb, C H Rodeck, K H Nicolaides, et al.
British Journal of Obstetrics and Gynaecology
|
December 1, 1983
Development of an improved technique for first-trimester microsampling of chorion
C H Rodeck, J M Morsman, C M Gosden, et al.
Fetal Diagnosis and Therapy
|
January 1, 1993
Fetal facial defects: associated malformations and chromosomal abnormalities
K H Nicolaides, D R Salvesen, R J Snijders, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
The British Journal of Radiology
|
October 1, 1990
Choroid plexus cysts and chromosomal defects
J G Thorpe-Beeston, C M Gosden, K H Nicolaides
American Journal of Obstetrics and Gynecology
|
February 1, 1993
Fetal growth retardation: associated malformations and chromosomal abnormalities
R J Snijders, C Sherrod, C M Gosden, et al.
American Journal of Human Genetics
|
September 1, 1993
De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier
D T Bonthron, S J Smith, J Fantes, et al.
Fetal Diagnosis and Therapy
|
January 1, 1992
Fetal nuchal oedema: associated malformations and chromosomal defects
K H Nicolaides, G Azar, R J Snijders, et al.
American Journal of Human Genetics
|
February 1, 1994
Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3
L Strain, C M Gosden, D J Brock, et al.
Human Genetics
|
April 1, 1988
Linkage heterogeneity and fragile X
J F Clayton, C M Gosden, N D Hastie, et al.
Clinical Genetics
|
June 1, 1979
Satellite DNA loss and nucleolar organiser activity in an individual with a de novo chromosome 13,14 translocation
J R Gosden, C M Gosden, S S Lawrie, et al.
Prenatal Diagnosis
|
March 1, 1987
Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid
T P Webb, C H Rodeck, K H Nicolaides, et al.
British Journal of Obstetrics and Gynaecology
|
December 1, 1983
Development of an improved technique for first-trimester microsampling of chorion
C H Rodeck, J M Morsman, C M Gosden, et al.
Fetal Diagnosis and Therapy
|
January 1, 1993
Fetal facial defects: associated malformations and chromosomal abnormalities
K H Nicolaides, D R Salvesen, R J Snijders, et al.
Page
of 6