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Results of search for 'au:"Lin, A E"', page 1 of 4
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Authors
Al-Jufan, M
Allanson, J
Amstutz, K S
Anderson, K R
Ardingen, H H
Ardinger, H H
Biglan, A W
Chin, A J
Clemens, M
Feingold, M
Garver, K L
Gorlin, R J
Graham, J M
Holmes, L B
Jaffe, R
Lacro, R V
Lin, A E
Losken, H W
Rosti, L
Westgate, M N
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Topics
Abnormalities, Multiple
Adolescent
Adult
Animals
Child
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Female
Heart Defects, Congenital
Humans
Infant
Infant, Newborn
Male
Phenotype
Pregnancy
Syndrome
abnormalities
complications
genetics
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English
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1.
Index of suspicion. Case 2.Turner's Syndrome.
[electronic resource]
by
Lin, A E
Producer:
19961226
In:
Pediatrics in review
vol. 17
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2.
Etiology of congenital heart defects.
[electronic resource]
by
Lin, A E
Producer:
19900711
In:
Pediatric pathology
vol. 10
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3.
Turner syndrome and hypoplastic left-heart syndrome.
[electronic resource]
by
Lin, A E
Producer:
19880307
In:
American journal of diseases of children (1960)
vol. 142
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4.
I heartily praise the first issue of Genetics in Medicine for its immediate applicability to clinical genetic practice.
[electronic resource]
by
Lin, A E
Producer:
20011101
In:
Genetics in medicine : official journal of the American College of Medical Genetics
vol. 1
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5.
Comments on "fetal coronary thrombosis and myocardial infarction ".
[electronic resource]
by
Lin, A E
Producer:
19911223
In:
Teratology
vol. 44
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6.
Prenatal ultrasound diagnosis of fetal scoliosis: spondylothoracic/spondylocostal dysplasia?
[electronic resource]
by
Lin, A E
Producer:
19890915
In:
Prenatal diagnosis
vol. 9
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7.
Airway foreign body.
[electronic resource]
by
Lin, A E
Producer:
19830107
In:
Clinical pediatrics
vol. 21
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8.
Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
[electronic resource]
by
Lin, A E
Producer:
19930730
In:
American journal of medical genetics
vol. 46
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9.
Two additional patients representing the possible human homologue for the mouse mutant disorganisation (Ds)
[electronic resource]
by
Lin, A E
Producer:
19911227
In:
Journal of medical genetics
vol. 28
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10.
Charge association vs. velo-cardio-facial syndrome.
[electronic resource]
by
Lin, A E
Producer:
19880831
In:
American journal of medical genetics
vol. 29
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11.
Maple syrup smell in the intensive care unit.
[electronic resource]
by
Lin, A E
Producer:
19820621
In:
Pediatrics
vol. 69
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12.
Using birth defects epidemiology to take CHARGE. Coloboma, Heart defect, choanal Atresia, Retardation, Genital, Ear anomaly.
[electronic resource]
by
Lin, A E
Producer:
20000106
In:
Teratology
vol. 60
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13.
Child-friendly healthcare initiative.
[electronic resource]
by
Lin, A E
Producer:
20020103
In:
Pediatrics
vol. 108
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14.
Chromosomal abnormality associated with congenital heart defect.
[electronic resource]
by
Lin, A E
Producer:
19900607
In:
American journal of medical genetics
vol. 35
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15.
Congenital heart defects in malformation syndromes.
[electronic resource]
by
Lin, A E
Producer:
19901206
In:
Clinics in perinatology
vol. 17
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16.
Pediatric cardiology.
[electronic resource]
by
Lin, A E
Producer:
19890131
In:
American journal of obstetrics and gynecology
vol. 159
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17.
Surgical and medical results of complete atrioventricular canal.
[electronic resource]
by
Lin, A E
Producer:
19880422
In:
The American journal of cardiology
vol. 61
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18.
Noonan syndrome.
[electronic resource]
by
Lin, A E
Producer:
19880425
In:
Journal of medical genetics
vol. 25
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19.
Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature.
[electronic resource]
by
Feingold, M
Lin, A E
Producer:
19940224
In:
American journal of medical genetics
vol. 47
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20.
Craniosynostosis, agenesis of the corpus callosum, serve mental retardation, distinctive facies, camptodactyly, and hypogonadism.
[electronic resource]
by
Lin, A E
Gettig, E
Producer:
19900607
In:
American journal of medical genetics
vol. 35
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