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Results of search for 'au:"Fryer, A E"', page 1 of 2
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Authors
Aasly, J O
Al-Gazali, L I
Arpa, J
Bacon, P
Barron, L
Black, G C
Bohlega, S
Brin, M
Cardy, A
Chalmers, A H
Clayton-Smith, J
Connor, J M
Fitzpatrick, D
Fryer, A E
Gilmour, M
Little, J
Mossey, P A
Osborne, J P
Povey, S
Webb, D W
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Cleft Lip
Cleft Palate
Female
Genetic Linkage
Humans
Infant
Infant, Newborn
Intellectual Disability
Male
Mutation
Pedigree
Tuberous Sclerosis
abnormalities
diagnosis
genetics
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English
Your search returned 28 results.
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1.
Tuberous sclerosis.
[electronic resource]
by
Fryer, A E
Producer:
19920305
In:
Journal of the Royal Society of Medicine
vol. 84
Online resources:
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2.
Clinical genetic services: activity, outcome, effectiveness and quality. Summary of a report of the Clinical Genetics Committee of The Royal College of Physicians.
[electronic resource]
by
Fryer, A E
Producer:
19980129
In:
Journal of the Royal College of Physicians of London
vol. 31
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3.
Scalp lipomas and cerebral malformations--report of a case and review of the literature.
[electronic resource]
by
Fryer, A E
Producer:
19940908
In:
Clinical dysmorphology
vol. 1
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4.
A patient with a previously undescribed overgrowth syndrome.
[electronic resource]
by
Fryer, A E
Producer:
19951106
In:
Clinical dysmorphology
vol. 4
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5.
Child with fronto-facio-nasal dysplasia, Hirschsprung's disease and hypospadias.
[electronic resource]
by
Fryer, A E
Producer:
19940217
In:
Clinical dysmorphology
vol. 2
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6.
Goldberg-Shprintzen syndrome: report of a new family and review of the literature.
[electronic resource]
by
Fryer, A E
Producer:
19980710
In:
Clinical dysmorphology
vol. 7
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7.
A new lethal skeletal dysplasia or the severe end of the atelosteogenesis spectrum?
[electronic resource]
by
Fryer, A E
Carty, H
Producer:
19961106
In:
Pediatric radiology
vol. 26
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8.
Recurrence of orbital cysts in the branchio-oculo-facial syndrome.
[electronic resource]
by
Fielding, D W
Fryer, A E
Producer:
19920731
In:
Journal of medical genetics
vol. 29
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9.
Forehead plaque: a presenting skin sign in tuberous sclerosis.
[electronic resource]
by
Fryer, A E
Osborne, J P
Schutt, W
Producer:
19870508
In:
Archives of disease in childhood
vol. 62
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10.
Trisomy 1 mosaicism only detected on a direct chromosome preparation in a neonate.
[electronic resource]
by
Howard, P J
Cramp, C E
Fryer, A E
Producer:
19961205
In:
Clinical genetics
vol. 48
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11.
On the incidence of fits and mental retardation in tuberous sclerosis.
[electronic resource]
by
Webb, D W
Fryer, A E
Osborne, J P
Producer:
19910913
In:
Journal of medical genetics
vol. 28
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12.
The cardio-facio-cutaneous (CFC) syndrome and Noonan syndrome: are they the same?
[electronic resource]
by
Fryer, A E
Holt, P J
Hughes, H E
Producer:
19910807
In:
American journal of medical genetics
vol. 38
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13.
Examining the parents of children with tuberous sclerosis.
[electronic resource]
by
Fryer, A E
Chalmers, A H
Osborne, J P
Producer:
19870121
In:
Lancet (London, England)
vol. 2
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14.
The value of investigation for genetic counselling in tuberous sclerosis.
[electronic resource]
by
Fryer, A E
Chalmers, A H
Osborne, J P
Producer:
19900523
In:
Journal of medical genetics
vol. 27
Online resources:
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15.
Morbidity associated with tuberous sclerosis: a population study.
[electronic resource]
by
Webb, D W
Fryer, A E
Osborne, J P
Producer:
19960510
In:
Developmental medicine and child neurology
vol. 38
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16.
Recurrence of Pallister-Hall syndrome in two sibs.
[electronic resource]
by
Thomas, H M
Todd, P J
Heaf, D
Fryer, A E
Producer:
19940616
In:
Journal of medical genetics
vol. 31
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17.
Tuberous sclerosis: a large family with no history of seizures or mental retardation.
[electronic resource]
by
Fryer, A E
Osborne, J P
Tan, R
Siggers, D C
Producer:
19871208
In:
Journal of medical genetics
vol. 24
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18.
Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndrome.
[electronic resource]
by
Fryer, A E
Upadhyaya, M
Littler, M
Bacon, P
Watkins, D
Tsipouras, P
Harper, P S
Producer:
19900507
In:
Journal of medical genetics
vol. 27
Online resources:
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19.
Genetic recombination between tuberous sclerosis and oncogene v-abl.
[electronic resource]
by
Povey, S
Burley, M W
Fryer, A E
Osborne, J
Al-Gazali, L I
Mueller, R
Producer:
19880825
In:
Lancet (London, England)
vol. 2
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20.
Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl.
[electronic resource]
by
Connor, J M
Pirrit, L A
Yates, J R
Fryer, A E
Ferguson-Smith, M A
Producer:
19871208
In:
Journal of medical genetics
vol. 24
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