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Results of search for 'au:"Baraitser, M"', page 6 of 10
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Authors
Baraitser, M
Brett, E M
Burn, J
Chitty, L S
Donnai, D
Fixsen, J
Hall, C M
Harbord, M G
Harding, A E
Harding, B
Hurst, J A
Kendall, B
Patton, M A
Reardon, W
Taylor, D
Temple, I K
Thompson, E
Thompson, E M
Wilson, J
Winter, R M
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Face
Female
Genes, Recessive
Humans
Infant
Infant, Newborn
Intellectual Disability
Male
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abnormalities
complications
diagnosis
genetics
pathology
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English
Your search returned 195 results.
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101.
The Holt-Oram syndrome.
[electronic resource]
by
Hurst, J A
Hall, C M
Baraitser, M
Producer:
19910913
In:
Journal of medical genetics
vol. 28
Online resources:
Available from publisher's website
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102.
Parietal foramina in Saethre-Chotzen syndrome.
[electronic resource]
by
Thompson, E M
Baraitser, M
Hayward, R D
Producer:
19850122
In:
Journal of medical genetics
vol. 21
Online resources:
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103.
Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?
[electronic resource]
by
Reardon, W
Temple, I K
Jones, B
Baraitser, M
Producer:
19901204
In:
Clinical genetics
vol. 38
Online resources:
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104.
The use of a computerised database for the diagnosis of a rare neurological syndrome.
[electronic resource]
by
Tomiwa, K
Baraitser, M
Brett, E M
Wilson, J
Producer:
19880225
In:
Neuropediatrics
vol. 18
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105.
Frontofacionasal dysplasia: a new case and review of the phenotype.
[electronic resource]
by
Reardon, W
Winter, R M
Taylor, D
Baraitser, M
Producer:
19940714
In:
Clinical dysmorphology
vol. 3
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106.
Atypical facio-scapulo-humeral muscular dystrophy--a counselling dilemma.
[electronic resource]
by
Reardon, W
Temple, I K
Harwood, G
Baraitser, M
Producer:
19910703
In:
Clinical genetics
vol. 39
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107.
Angelman's syndrome.
[electronic resource]
by
Scheffer, I
Brett, E M
Wilson, J
Baraitser, M
Producer:
19900523
In:
Journal of medical genetics
vol. 27
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108.
Biochemical and clinical studies of Friedreich's ataxia.
[electronic resource]
by
Purkiss, P
Baraitser, M
Borud, O
Chalmers, R A
Producer:
19811221
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 44
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109.
A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection.
[electronic resource]
by
Burn, J
Wickramasinghe, H T
Harding, B
Baraitser, M
Producer:
19861114
In:
Clinical genetics
vol. 30
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110.
Trigonocephaly and the Opitz C syndrome.
[electronic resource]
by
Sargent, C
Burn, J
Baraitser, M
Pembrey, M E
Producer:
19850426
In:
Journal of medical genetics
vol. 22
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111.
A case of atelosteogenesis.
[electronic resource]
by
Temple, K
Hall, C A
Chitty, L
Baraitser, M
Producer:
19900515
In:
Journal of medical genetics
vol. 27
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112.
Orofaciodigital syndrome with mesomelic limb shortening.
[electronic resource]
by
Burn, J
Dezateux, C
Hall, C M
Baraitser, M
Producer:
19840824
In:
Journal of medical genetics
vol. 21
Online resources:
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113.
Mental retardation, microcephaly and blepharochalasis in brothers.
[electronic resource]
by
Reardon, W
Winter, R M
Wilson, J
Baraitser, M
Producer:
19940912
In:
Clinical dysmorphology
vol. 3
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114.
Total situs inversus associated with the oculo-auriculo-vertebral spectrum.
[electronic resource]
by
Maat-Kievit, J A
Baraitser, M
Winter, R M
Producer:
19940714
In:
Clinical dysmorphology
vol. 3
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115.
Hemihypertrophy, hemimegalencephaly, and polydactyly.
[electronic resource]
by
Reardon, W
Harding, B
Winter, R M
Baraitser, M
Producer:
19970225
In:
American journal of medical genetics
vol. 66
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116.
Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?
[electronic resource]
by
Reardon, W
Hall, C M
Dillon, M J
Baraitser, M
Producer:
19911227
In:
Journal of medical genetics
vol. 28
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117.
Organic acidurias and amino acidurias in the aetiology of long-term mental handicap.
[electronic resource]
by
Watts, R W
Baraitser, M
Chalmers, R A
Purkiss, P
Producer:
19810625
In:
Journal of mental deficiency research
vol. 24 Pt 4
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118.
Distal spinal muscular atrophy with vocal cord paralysis.
[electronic resource]
by
Pridmore, C
Baraitser, M
Brett, E M
Harding, A E
Producer:
19920428
In:
Journal of medical genetics
vol. 29
Online resources:
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119.
Axonal velocities of motor units in the hand and foot muscles of the baboon.
[electronic resource]
by
Gilliatt, R W
Hopf, H C
Rudge, P
Baraitser, M
Producer:
19761223
In:
Journal of the neurological sciences
vol. 29
Online resources:
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120.
A distinctive type of hypohidrotic ectodermal dysplasia featuring hypothyroidism.
[electronic resource]
by
Pike, M G
Baraitser, M
Dinwiddie, R
Atherton, D J
Producer:
19860228
In:
The Journal of pediatrics
vol. 108
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