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Results of search for 'au:"Blank, C E"', page 1 of 2
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Authors
Atherton, G W
BISHOP, A
BISHOP, A M
BLANK, C E
BOND, J H
Bishop, A M
Blank, C E
CASEY, M D
Casey, M D
Curtis, D
DEWHURST, C J
Dewhurst, C J
Hughes, H N
Issa, M
Johnson, M
Kumar, D
Lorber, J
Parsons, M A
Potter, A M
Street, D R
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Chromosomes
Dermatoglyphics
Disorders of Sex Development
Down Syndrome
Female
Humans
Infant
Intellectual Disability
Karyotyping
Male
Pedigree
Sex Chromatin
genetics
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English
Your search returned 40 results.
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1.
Chromosome abnormalities in man. Three types of chromosome abnormality and their clinical significance.
[electronic resource]
by
Blank, C E
Producer:
19671121
In:
Igaku to seibutsugaku. Medicine and biology
vol. 73
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2.
Chromosome abnormality in mongolism.
[electronic resource]
by
BLANK, C E
Producer:
19981101
In:
Proceedings of the Royal Society of Medicine
vol. 55
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3.
SOME ASPECTS OF CHROMOSOME MOSAICISM IN CLINICAL MEDICINE.
[electronic resource]
by
BLANK, C E
Producer:
19961201
In:
Lancet (London, England)
vol. 2
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4.
Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases.
[electronic resource]
by
BLANK, C E
Producer:
19981101
In:
Annals of human genetics
vol. 24
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5.
Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30320).
[electronic resource]
by
Curtis, D
Blank, C E
Producer:
19890306
In:
Human genetics
vol. 81
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6.
A patient with 45,XX,Gminus-46,XX,Gr mosaicism.
[electronic resource]
by
Blank, C E
Lorber, J
Producer:
19690930
In:
Journal of medical genetics
vol. 6
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7.
Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.
[electronic resource]
by
Kumar, D
Blank, C E
Producer:
19900510
In:
Indian pediatrics
vol. 26
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8.
Timing of morphological and ecological innovations in the cyanobacteria--a key to understanding the rise in atmospheric oxygen.
[electronic resource]
by
Blank, C E
Sánchez-Baracaldo, P
Producer:
20100310
In:
Geobiology
vol. 8
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9.
Family with neuromuscular disorder where mode of inheritance was resolved by RFLP analysis.
[electronic resource]
by
Blank, C E
Curtis, D J
Producer:
19870302
In:
Lancet (London, England)
vol. 1
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10.
Absorption and circular dichroism studies of a gold (I)-DNA complex.
[electronic resource]
by
Blank, C E
Dabrowiak, J C
Producer:
19840713
In:
Journal of inorganic biochemistry
vol. 21
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11.
An evaluation of reinforcement of genetic counselling on the consultand.
[electronic resource]
by
Curtis, D
Johnson, M
Blank, C E
Producer:
19880602
In:
Clinical genetics
vol. 33
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12.
Hereditary cerebellar ataxia and genetic linkage with HLA.
[electronic resource]
by
Kumar, D
Blank, C E
Gelsthorpe, K
Producer:
19860612
In:
Human genetics
vol. 72
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13.
Grebe chondrodysplasia and brachydactyly in a family.
[electronic resource]
by
Kumar, D
Curtis, D
Blank, C E
Producer:
19840518
In:
Clinical genetics
vol. 25
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14.
THE RELATIVE LENGTH AND ARM RATIO OF THE HUMAN LATE-REPLICATING X CHROMOSOME.
[electronic resource]
by
BISHOP, A
LEESE, M
BLANK, C E
Producer:
19961201
In:
Journal of medical genetics
vol. 2
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15.
Multivitamins and prevention of neural tube defects: a need for detailed counselling.
[electronic resource]
by
Blank, C E
Kumar, D
Johnson, M
Producer:
19840504
In:
Lancet (London, England)
vol. 1
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16.
Multiple congenital defects associated with trisomy for long arm of No. 4.
[electronic resource]
by
Issa, M
Potter, A M
Blank, C E
Producer:
19761029
In:
Journal of medical genetics
vol. 13
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17.
Investigations for genotoxic effects after exposure to crude 2,4,5-trichlorophenol.
[electronic resource]
by
Blank, C E
Cooke, P
Potter, A M
Producer:
19830407
In:
British journal of industrial medicine
vol. 40
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18.
Clinical manifestations of trisomy 5q.
[electronic resource]
by
Kumar, D
Heath, P R
Blank, C E
Producer:
19870612
In:
Journal of medical genetics
vol. 24
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19.
The temporal appearance of sex chromatin and of the late-replicating X chromosome in blastocysts of the domestic rabbit.
[electronic resource]
by
Issa, M
Blank, C E
Atherton, G W
Producer:
19690930
In:
Cytogenetics
vol. 8
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20.
Cornelia de Lange syndrome in several members of the same family.
[electronic resource]
by
Kumar, D
Blank, C E
Griffiths, B L
Producer:
19851031
In:
Journal of medical genetics
vol. 22
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