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Results of search for 'au:"Pober, B"', page 1 of 3
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Authors
Ballabio, A
Bennett, M J
Bodurtha, J
Bruttini, M
Cherniske, E M
Costa, T
Donahoe, P K
Doubilet, P M
Gibson, L H
Graham, J M
Holmes, L B
Jonsson, J J
Kashtan, C E
Osborne, L R
Piccini, M
Pober, B
Pober, B R
Renieri, A
Scherer, S W
Tsui, L C
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Deletion
Chromosome Mapping
Female
Humans
Infant
Infant, Newborn
Male
Molecular Sequence Data
Phenotype
Syndrome
Williams Syndrome
abnormalities
complications
diagnosis
genetics
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English
Your search returned 47 results.
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1.
Genetic aspects of human congenital diaphragmatic hernia.
[electronic resource]
by
Pober, B R
Producer:
20080926
In:
Clinical genetics
vol. 74
Online resources:
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2.
Genetics of childhood disorders: XXVII. Genes and cognition in Williams syndrome.
[electronic resource]
by
Osborne, L
Pober, B
Producer:
20010726
In:
Journal of the American Academy of Child and Adolescent Psychiatry
vol. 40
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3.
Association of Chiari I malformation and Williams syndrome.
[electronic resource]
by
Pober, B R
Filiano, J J
Producer:
19950621
In:
Pediatric neurology
vol. 12
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4.
Genetics of childhood disorders: XXVI. Williams syndrome and brain-behavior relationships.
[electronic resource]
by
Schultz, R T
Grelotti, D J
Pober, B
Producer:
20010712
In:
Journal of the American Academy of Child and Adolescent Psychiatry
vol. 40
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5.
Williams syndrome--oral presentation of 45 cases.
[electronic resource]
by
Hertzberg, J
Nakisbendi, L
Needleman, H L
Pober, B
Producer:
19941116
In:
Pediatric dentistry
vol. 16
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6.
Type III tracheal agenesis with familial tetralogy of Fallot and absent pulmonary valve syndrome.
[electronic resource]
by
Hirt-Armon, K
Pober, B R
Holmes, L B
Producer:
19970221
In:
American journal of medical genetics
vol. 65
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7.
Neurologic findings in children and adults with Williams syndrome.
[electronic resource]
by
Chapman, C A
du Plessis, A
Pober, B R
Producer:
19961004
In:
Journal of child neurology
vol. 11
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8.
Description of common musculoskeletal findings in Williams Syndrome and implications for therapies.
[electronic resource]
by
Copes, L E
Pober, B R
Terilli, C A
Producer:
20170206
In:
Clinical anatomy (New York, N.Y.)
vol. 29
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9.
Smoking and pregnancy.
[electronic resource]
by
Werler, M M
Pober, B R
Holmes, L B
Producer:
19860207
In:
Teratology
vol. 32
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10.
Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities.
[electronic resource]
by
Shapira, S K
Neish, A S
Pober, B R
Producer:
19920828
In:
Journal of medical genetics
vol. 29
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11.
Accuracy of fetal echocardiography.
[electronic resource]
by
Benacerraf, B R
Pober, B R
Sanders, S P
Producer:
19871229
In:
Radiology
vol. 165
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12.
Complexities of intraventricular abnormalities.
[electronic resource]
by
Pober, B R
Greene, M F
Holmes, L B
Producer:
19860430
In:
The Journal of pediatrics
vol. 108
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13.
A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.
[electronic resource]
by
Lin, C L
Gibson, L
Pober, B
Yang-Feng, T L
Producer:
19960131
In:
Human genetics
vol. 96
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14.
Reporting accuracy among mothers of malformed and nonmalformed infants.
[electronic resource]
by
Werler, M M
Pober, B R
Nelson, K
Holmes, L B
Producer:
19890214
In:
American journal of epidemiology
vol. 129
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15.
Elevated ambulatory blood pressure in 20 subjects with Williams syndrome.
[electronic resource]
by
Broder, K
Reinhardt, E
Ahern, J
Lifton, R
Tamborlane, W
Pober, B
Producer:
19990707
In:
American journal of medical genetics
vol. 83
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16.
Sonography of Nager acrofacial dysostosis syndrome in utero.
[electronic resource]
by
Benson, C B
Pober, B R
Hirsh, M P
Doubilet, P M
Producer:
19880503
In:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
vol. 7
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17.
Acrocallosal syndrome: new findings.
[electronic resource]
by
Moeschler, J B
Pober, B R
Holmes, L B
Graham, J M
Producer:
19890630
In:
American journal of medical genetics
vol. 32
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18.
The neuropathology of Williams syndrome. Report of a 35-year-old man with presenile beta/A4 amyloid plaques and neurofibrillary tangles.
[electronic resource]
by
Golden, J A
Nielsen, G P
Pober, B R
Hyman, B T
Producer:
19950308
In:
Archives of neurology
vol. 52
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19.
Isolated congenital renal tubular immaturity in siblings.
[electronic resource]
by
Schwartz, B R
Lage, J M
Pober, B R
Driscoll, S G
Producer:
19870202
In:
Human pathology
vol. 17
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20.
Renal findings in 40 individuals with Williams syndrome.
[electronic resource]
by
Pober, B R
Lacro, R V
Rice, C
Mandell, V
Teele, R L
Producer:
19930610
In:
American journal of medical genetics
vol. 46
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