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Results of search for 'au:"Baraitser, M"', page 1 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
Pedigree
Syndrome
abnormalities
complications
diagnosis
genetics
pathology
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English
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1.
Genetic aspects of speech disorders.
[electronic resource]
by
Baraitser, M
Producer:
19871127
In:
Journal of tropical pediatrics
vol. 33
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2.
The orofaciodigital (OFD) syndromes.
[electronic resource]
by
Baraitser, M
Producer:
19860627
In:
Journal of medical genetics
vol. 23
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3.
The hypertelorism microtia clefting syndrome.
[electronic resource]
by
Baraitser, M
Producer:
19830119
In:
Journal of medical genetics
vol. 19
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4.
Children who look different.
[electronic resource]
by
Baraitser, M
Producer:
19881013
In:
Midwife, health visitor & community nurse
vol. 24
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5.
Relevance of a family history of seizures.
[electronic resource]
by
Baraitser, M
Producer:
19830729
In:
Archives of disease in childhood
vol. 58
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6.
The genetics of the spinal muscular atrophies.
[electronic resource]
by
Baraitser, M
Producer:
19890801
In:
Progress in clinical and biological research
vol. 306
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7.
Chromosomes and mental retardation.
[electronic resource]
by
Baraitser, M
Producer:
19861118
In:
Psychological medicine
vol. 16
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8.
Genetics of Möbius syndrome.
[electronic resource]
by
Baraitser, M
Producer:
19780417
In:
Journal of medical genetics
vol. 14
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9.
A new camptodactyly syndrome.
[electronic resource]
by
Baraitser, M
Producer:
19820621
In:
Journal of medical genetics
vol. 19
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10.
Marshall/Stickler syndrome.
[electronic resource]
by
Baraitser, M
Producer:
19820708
In:
Journal of medical genetics
vol. 19
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11.
Coffin-Siris syndrome.
[electronic resource]
by
Levy, P
Baraitser, M
Producer:
19910906
In:
Journal of medical genetics
vol. 28
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12.
Brief clinical report: neural tube defects as an X-linked condition.
[electronic resource]
by
Baraitser, M
Burn, J
Producer:
19840511
In:
American journal of medical genetics
vol. 17
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13.
Primidone teratogenicity or Noonan syndrome?
[electronic resource]
by
Burn, J
Baraitser, M
Producer:
19820624
In:
The Journal of pediatrics
vol. 100
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14.
A single maxillary incisor as a manifestation of an ectodermal dysplasia.
[electronic resource]
by
Buntinx, I
Baraitser, M
Producer:
19900110
In:
Journal of medical genetics
vol. 26
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15.
Neurological complications in one of a sibpair with aplasia cutis congenita.
[electronic resource]
by
Ho, C
Baraitser, M
Producer:
19940218
In:
Clinical dysmorphology
vol. 1
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16.
Nosology of Smith-Lemli-Opitz syndrome.
[electronic resource]
by
Thompson, E
Baraitser, M
Producer:
19880212
In:
American journal of medical genetics
vol. 28
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17.
Partial lipoatrophy with insulin resistant diabetes and hyperlipidaemia (Dunnigan syndrome).
[electronic resource]
by
Burn, J
Baraitser, M
Producer:
19860627
In:
Journal of medical genetics
vol. 23
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18.
FG syndrome.
[electronic resource]
by
Thompson, E
Baraitser, M
Producer:
19870612
In:
Journal of medical genetics
vol. 24
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19.
Recently recognized chromosomal defects of clinical importance.
[electronic resource]
by
Pembrey, M
Baraitser, M
Producer:
19870219
In:
Postgraduate medical journal
vol. 62
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20.
An autosomal recessive mental retardation syndrome with hepatic fibrosis and renal cysts.
[electronic resource]
by
Thompson, E
Baraitser, M
Producer:
19860530
In:
American journal of medical genetics
vol. 24
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