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Results of search for 'au:"Duckett, D P"', page 1 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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1.
Proximal 15q monosomy.
[electronic resource]
by
Duckett, D P
Producer:
19830119
In:
Journal of medical genetics
vol. 19
Online resources:
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2.
A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion.
[electronic resource]
by
Duckett, D P
Young, I D
Producer:
19880914
In:
Human genetics
vol. 79
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3.
A new pericentric inversion of chromosome 6 in an abnormal infant.
[electronic resource]
by
Duckett, D P
Roberts, S H
Producer:
19800926
In:
Annales de genetique
vol. 23
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4.
Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.
[electronic resource]
by
Roberts, S H
Duckett, D P
Producer:
19790425
In:
Journal of medical genetics
vol. 15
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5.
Familial cerebellar ataxia and possible cosegregation with an inversion in chromosome 4.
[electronic resource]
by
Young, I D
Duckett, D P
Producer:
19900713
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 53
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6.
Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.
[electronic resource]
by
Duckett, D P
Roberts, S H
Producer:
19820412
In:
Human genetics
vol. 58
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7.
Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.
[electronic resource]
by
Duckett, D P
Roberts, S H
Davies, P
Producer:
19840919
In:
Human genetics
vol. 67
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8.
Maternal cell contamination in chorionic villus samples assessed by direct preparations and three different culture methods.
[electronic resource]
by
Roberts, E
Duckett, D P
Lang, G D
Producer:
19890216
In:
Prenatal diagnosis
vol. 8
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9.
Behaviour disorder in monosomy 10qter.
[electronic resource]
by
Mehta, L
Duckett, D P
Young, I D
Producer:
19870612
In:
Journal of medical genetics
vol. 24
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10.
Lethal presentation of mosaic tetrasomy 12p (Pallister-Killian) syndrome.
[electronic resource]
by
Young, I D
Duckett, D P
O'Reilly, K M
Producer:
19890814
In:
Annales de genetique
vol. 32
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11.
Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
[electronic resource]
by
Duckett, D P
Porter, H J
Young, I D
Producer:
19921015
In:
Annales de genetique
vol. 35
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12.
Prenatal diagnosis of trisomy for the distal two-thirds of the long arm of chromosome 14 (q21----qter).
[electronic resource]
by
Duckett, D P
Roberts, E
McKeever, P
Young, I D
Producer:
19900813
In:
Prenatal diagnosis
vol. 10
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13.
Trisomy 18 in a 13 year old girl.
[electronic resource]
by
Mehta, L
Shannon, R S
Duckett, D P
Young, I D
Producer:
19860725
In:
Journal of medical genetics
vol. 23
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14.
Ocular findings in Angelman's (happy puppet) syndrome.
[electronic resource]
by
Dickinson, A J
Fielder, A R
Young, I D
Duckett, D P
Producer:
19900711
In:
Ophthalmic paediatrics and genetics
vol. 11
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15.
Recurrent spontaneous abortions due to a homologous Robertsonian translocation (14q14q).
[electronic resource]
by
Gracias-Espinal, R
Roberts, S H
Duckett, D P
Laurence, K M
Producer:
19830317
In:
Journal of medical genetics
vol. 19
Online resources:
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16.
Origin of the X chromosomes in a patient with the 49,XXXXY syndrome.
[electronic resource]
by
Plaha, D S
Duckett, D P
Collacott, R A
Young, I D
Producer:
19900515
In:
Journal of medical genetics
vol. 27
Online resources:
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17.
Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysis.
[electronic resource]
by
Dalgleish, R
Duckett, D P
Woodhouse, M
Shannon, R S
Young, I D
Producer:
19890421
In:
Journal of medical genetics
vol. 25
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18.
Down's syndrome and fragile-X syndrome in a single patient.
[electronic resource]
by
Collacott, R A
Duckett, D P
Mathews, D
Warrington, J S
Young, I D
Producer:
19900514
In:
Journal of mental deficiency research
vol. 34 ( Pt 1)
Online resources:
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19.
Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
[electronic resource]
by
Long, F L
Duckett, D P
Billam, L J
Williams, D K
Crolla, J A
Producer:
19980729
In:
Journal of medical genetics
vol. 35
Online resources:
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20.
Three-base pair resolution of DNA fragments on agarose: application to delta F508 analysis in cystic fibrosis.
[electronic resource]
by
Plaha, D S
Linforth, G H
Duckett, D P
Scott-Jupp, R
Tanner, M S
Jeffreys, A J
Producer:
19930527
In:
BioTechniques
vol. 14
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