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Results of search for 'au:"Zackai, E H"', page 1 of 9
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Authors
Budarf, M L
Celle, L
Clark, B J
Driscoll, D A
Emanuel, B S
Eunpu, D L
Gerdes, M
Goldmuntz, E
Gripp, K W
McDonald-McGinn, D
McDonald-McGinn, D M
Mennuti, M T
Ming, J E
Muenke, M
Overhauser, J
Robin, N H
Schnur, R E
Solot, C
Spinner, N B
Zackai, E H
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 22
Female
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Karyotyping
Male
Pedigree
Phenotype
Syndrome
abnormalities
diagnosis
genetics
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English
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1.
Deletion 4q34.2.
[electronic resource]
by
Zackai, E H
Producer:
19991001
In:
American journal of medical genetics
vol. 86
Online resources:
Available from publisher's website
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2.
Gene location in neurofibromatosis.
[electronic resource]
by
Stambolian, D
Zackai, E H
Producer:
19880831
In:
American journal of medical genetics
vol. 29
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3.
A new twist: some patients with Saethre-Chotzen syndrome have a microdeletion syndrome.
[electronic resource]
by
Zackai, E H
Stolle, C A
Producer:
19981223
In:
American journal of human genetics
vol. 63
Online resources:
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4.
Ring chromosome 7 with variable phenotypic expression.
[electronic resource]
by
Zackai, E H
Breg, W R
Producer:
19730731
In:
Cytogenetics and cell genetics
vol. 12
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5.
Unusual craniofacial dysmorphia due to prenatal alcohol and cocaine exposure.
[electronic resource]
by
Robin, N H
Zackai, E H
Producer:
19950125
In:
Teratology
vol. 50
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6.
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.
[electronic resource]
by
Zackai, E H
Emanuel, B S
Producer:
19810521
In:
American journal of medical genetics
vol. 7
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7.
Circumferential ringed creases ("Michelin tire babies") with specific histologic findings and/or karyotype abnormalities: clues to molecular pathogenesis?
[electronic resource]
by
Schnur, R E
Zackai, E H
Producer:
19970508
In:
American journal of medical genetics
vol. 69
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8.
Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.
[electronic resource]
by
Münke, M
Emanuel, B S
Zackai, E H
Producer:
19881207
In:
American journal of medical genetics
vol. 30
Online resources:
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9.
Thrombocytopenia with absent radius in a boy and his uncle.
[electronic resource]
by
Schnur, R E
Eunpu, D L
Zackai, E H
Producer:
19871203
In:
American journal of medical genetics
vol. 28
Online resources:
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10.
Microcephaly, mild mental retardation, short stature, and skeletal anomalies in siblings.
[electronic resource]
by
Zackai, E H
Sly, W S
McAlister, W G
Producer:
19720811
In:
American journal of diseases of children (1960)
vol. 124
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11.
What's in a name? The 22q11.2 deletion.
[electronic resource]
by
McDonald-McGinn, D M
Zackai, E H
Low, D
Producer:
19971112
In:
American journal of medical genetics
vol. 72
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12.
Trisomy 21: rate in second-degree relatives.
[electronic resource]
by
Eunpu, D L
McDonald, D M
Zackai, E H
Producer:
19861210
In:
American journal of medical genetics
vol. 25
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13.
The diagnosis of neurofibromatosis-1 in the child under the age of 6 years.
[electronic resource]
by
Obringer, A C
Meadows, A T
Zackai, E H
Producer:
19890710
In:
American journal of diseases of children (1960)
vol. 143
Online resources:
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14.
Not Antley-Bixler syndrome.
[electronic resource]
by
Gripp, K W
Zackai, E H
Cohen, M M
Producer:
19990527
In:
American journal of medical genetics
vol. 83
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15.
The Neurofibromatosis Clinic of the Children's Hospital of Philadelphia.
[electronic resource]
by
Obringer, A C
Zackai, E H
Meadows, A T
Producer:
19900502
In:
Neurofibromatosis
vol. 1
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16.
Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
[electronic resource]
by
Emanuel, B S
Zackai, E H
Tucker, S H
Producer:
19840214
In:
Journal of medical genetics
vol. 20
Online resources:
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17.
Neural tube defects, diabetes, and serum alpha-fetoprotein screening.
[electronic resource]
by
Eunpu, D L
Zackai, E H
Mennuti, M T
Producer:
19831217
In:
American journal of obstetrics and gynecology
vol. 147
Online resources:
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18.
High cesarean section rate in trisomy 18 births: a potential indication for late prenatal diagnosis.
[electronic resource]
by
Schneider, A S
Mennuti, M T
Zackai, E H
Producer:
19810810
In:
American journal of obstetrics and gynecology
vol. 140
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19.
Congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation: the Schinzel-Giedion syndrome.
[electronic resource]
by
Kelley, R I
Zackai, E H
Charney, E B
Producer:
19820826
In:
The Journal of pediatrics
vol. 100
Online resources:
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20.
Mutations in the human TWIST gene.
[electronic resource]
by
Gripp, K W
Zackai, E H
Stolle, C A
Producer:
20000224
In:
Human mutation
vol. 15
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