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Lancet (London, England)|February 8, 1986
Rapid karyotyping in non-lethal fetal malformationsK H Nicolaides, C H Rodeck, C M GosdenAmerican Journal of Human Genetics|March 1, 1981
Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphismsJ R Gosden, S S Lawrie, C M GosdenFetal Therapy|January 1, 1989
Prenatal diagnosis of congenital diaphragmatic hernia: associated malformations and chromosomal defectsJ G Thorpe-Beeston, C M Gosden, K H NicolaidesThe British Journal of Radiology|October 1, 1990
Choroid plexus cysts and chromosomal defectsJ G Thorpe-Beeston, C M Gosden, K H NicolaidesAmerican Journal of Obstetrics and Gynecology|February 1, 1993
Fetal growth retardation: associated malformations and chromosomal abnormalitiesR 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 carrierD T Bonthron, S J Smith, J Fantes, et al.Fetal Diagnosis and Therapy|January 1, 1992
Fetal nuchal oedema: associated malformations and chromosomal defectsK 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 Xq27.3L Strain, C M Gosden, D J Brock, et al.Human Genetics|April 1, 1988
Linkage heterogeneity and fragile XJ 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 translocationJ R Gosden, C M Gosden, S S Lawrie, et al.Pageof 9