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Results of search for 'au:"Willey, A M"'
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Authors
Barron, K D
Cross, P K
Csiza, C K
Dearborn, R E
Hatcher, N H
Healy, N P
Hook, E B
Hurwitz, C G
Koeppen, A H
Mottironi, V D
Porter, I H
Rønne, M
Schreinemachers, D M
Swift, R V
Willey, A M
Yunis, J J
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Topics
Abortion, Induced
Adult
Amniocentesis
Animals
Autoradiography
Birth Rate
Chromosome Aberrations
Female
Gene Frequency
Humans
Karyotyping
Male
Maternal Age
Middle Aged
Mutation
New York
Pregnancy
Prenatal Diagnosis
Translocation, Genetic
United States
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English
Your search returned 7 results.
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1.
Localization and characterization of the repetitive DNA of the Algerian hedgehog, Erinaceus (Aethecinus) algirus. I.
[electronic resource]
by
Willey, A M
Yunis, J J
Producer:
19750807
In:
Experimental cell research
vol. 91
Availability:
No items available.
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2.
Abortions because of unavailability of prenatal diagnosis.
[electronic resource]
by
Hook, E B
Willey, A M
Producer:
19820128
In:
Lancet (London, England)
vol. 2
Availability:
No items available.
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3.
How much difference does chromosome banding make? Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities.
[electronic resource]
by
Hook, E B
Healy, N P
Willey, A M
Producer:
19900124
In:
Annals of human genetics
vol. 53
Online resources:
Available from publisher's website
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No items available.
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4.
Rates of mutant structural chromosome rearrangements in human fetuses: data from prenatal cytogenetic studies and associations with maternal age and parental mutagen exposure.
[electronic resource]
by
Hook, E B
Schreinemachers, D M
Willey, A M
Cross, P K
Producer:
19830324
In:
American journal of human genetics
vol. 35
Availability:
No items available.
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5.
Inherited structural cytogenetic abnormalities detected incidentally in fetuses diagnosed prenatally: frequency, parental-age associations, sex-ratio trends, and comparisons with rates of mutants.
[electronic resource]
by
Hook, E B
Schreinemachers, D M
Willey, A M
Cross, P K
Producer:
19840502
In:
American journal of human genetics
vol. 36
Availability:
No items available.
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6.
Decreased HLA heterogeneity in parents of children with Down syndrome.
[electronic resource]
by
Mottironi, V D
Hook, E B
Willey, A M
Porter, I H
Swift, R V
Hatcher, N H
Producer:
19840107
In:
American journal of human genetics
vol. 35
Availability:
No items available.
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7.
Myelin deficiency in female rats due to a mutation in the PLP gene.
[electronic resource]
by
Koeppen, A H
Csiza, C K
Willey, A M
Rønne, M
Barron, K D
Dearborn, R E
Hurwitz, C G
Producer:
19920609
In:
Journal of the neurological sciences
vol. 107
Online resources:
Available from publisher's website
Availability:
No items available.
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