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Results of search for 'au:"Duckett, D P"', page 2 of 2
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Authors
Barrow, M A
Billam, L J
Braddock, D
Brenchley, P
Collacott, R A
Crolla, J A
D'Souza, S W
Dalgleish, R
Davies, P
De Chazal, R C
Dickinson, A J
Duckett, D P
Konje, J C
Mehta, L
Plaha, D S
Roberts, E
Roberts, S H
Shannon, R S
Taylor, D J
Young, I D
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Topics
Abnormalities, Multiple
Adolescent
Adult
Amniocentesis
Child
Child, Preschool
Chromosome Aberrations
Chromosome Deletion
Chromosomes, Human, 13-15
Female
Humans
Intellectual Disability
Karyotyping
Male
Pedigree
Phenotype
Pregnancy
Translocation, Genetic
Trisomy
genetics
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English
Your search returned 24 results.
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21.
Invasive testing for the karyotyping of mid-trimester intrauterine fetal death (IUFD): a pilot study.
[electronic resource]
by
Howarth, E S
Konje, J C
Healey, K A
Duckett, D P
Scudamore, I W
Taylor, D J
Producer:
20021220
In:
Prenatal diagnosis
vol. 22
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22.
Expression of LFA-1 by a lymphoblastoid cell line from a patient with monosomy 21: effects on intercellular adhesion.
[electronic resource]
by
Taylor, G M
Braddock, D
Robson, A J
Fergusson, W D
Duckett, D P
D'Souza, S W
Brenchley, P
Producer:
19901018
In:
Clinical and experimental immunology
vol. 81
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23.
Genetic amniocentesis: gestation-specific pregnancy outcome and comparison of outcome following early and traditional amniocentesis.
[electronic resource]
by
Roper, E C
Konje, J C
De Chazal, R C
Duckett, D P
Oppenheimer, C A
Taylor, D J
Producer:
19991118
In:
Prenatal diagnosis
vol. 19
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24.
Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.
[electronic resource]
by
Wilson, L C
Leverton, K
Oude Luttikhuis, M E
Oley, C A
Flint, J
Wolstenholme, J
Duckett, D P
Barrow, M A
Leonard, J V
Read, A P
Producer:
19950309
In:
American journal of human genetics
vol. 56
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