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Results of search for 'au:"KABACK, M M"', page 2 of 5
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Authors
Akerman, B R
Becker, M H
Campion, D S
Cantor, R M
Desnick, R J
Greenwald, S
Herndon, R M
Howell, R R
Kaback, M M
Kazazian, H H
Leisti, J
Lim, J S
Mohandas, T
Nathan, T J
Natowicz, M R
Neufeld, E F
Percy, A K
Rimoin, D L
Roy, C
Shapiro, L J
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Topics
Adolescent
Adult
Amniocentesis
Child, Preschool
Female
Genetic Carrier Screening
Genetic Counseling
Genetic Testing
Heterozygote
Humans
Jews
Lipidoses
Male
Pregnancy
Tay-Sachs Disease
beta-N-Acetylhexosaminidases
diagnosis
enzymology
genetics
metabolism
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English
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21.
Infantile metachromatic leukodystrophy.
[electronic resource]
by
Kaback, M M
Howell, R R
Producer:
19700701
In:
The New England journal of medicine
vol. 282
Online resources:
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22.
Tay-Sachs disease: from clinical description to molecular defect.
[electronic resource]
by
Kaback, M M
Desnick, R J
Producer:
20020307
In:
Advances in genetics
vol. 44
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23.
The Turner phenotype associated with unbalanced X/autosome translocation.
[electronic resource]
by
Leisti, J
Kaback, M M
Rimoin, D L
Producer:
19760525
In:
Birth defects original article series
vol. 11
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24.
Chromosome polymorphisms in karyotypes from amniotic fluid cell cultures.
[electronic resource]
by
Barker, P E
Mohandas, T
Kaback, M M
Producer:
19770611
In:
Clinical genetics
vol. 11
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25.
Tay-Sachs disease: heterozygote screening and prenatal diagnosis--U.S. experience and world perspective.
[electronic resource]
by
Kaback, M M
Nathan, T J
Greenwald, S
Producer:
19780329
In:
Progress in clinical and biological research
vol. 18
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26.
THE EFFECT OF 5-BROMODEOXYURIDINE ON HUMAN CHROMOSOMES.
[electronic resource]
by
KABACK, M M
SAKSELA, E
MELLMAN, W J
Producer:
19961201
In:
Experimental cell research
vol. 34
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27.
Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation.
[electronic resource]
by
Leisti, J
Kaback, M M
Rimoin, D L
Producer:
19760525
In:
Birth defects original article series
vol. 11
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28.
Uroporphyrinogen 3 cosynthetase activity in fibroblasts from patients with congenital erythropoietic porphyria.
[electronic resource]
by
Romeo, G
Kaback, M M
Levin, E Y
Producer:
19710311
In:
Biochemical genetics
vol. 4
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29.
Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection.
[electronic resource]
by
Howell, R R
Kaback, M M
Brown, B I
Producer:
19710426
In:
The Journal of pediatrics
vol. 78
Online resources:
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30.
Sociologic studies in human genetics. I. Compliance factors in a voluntary heterozygote screening program.
[electronic resource]
by
Kaback, M M
Becker, M H
Ruth, M V
Producer:
19760324
In:
Birth defects original article series
vol. 10
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31.
Tay-Sachs disease: one-step assay of beta-N-acetylhexosaminidase in serum with a sulphated chromogenic substrate.
[electronic resource]
by
Fuchs, W
Navon, R
Kaback, M M
Kresse, H
Producer:
19831220
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 133
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32.
Automated thermal fractionation of serum hexosaminidase: effects of alteration in reaction variables and implications for Tay-Sachs disease heterozygote screening.
[electronic resource]
by
Kaback, M M
Bailin, G
Hirsch, P
Roy, C
Producer:
19780329
In:
Progress in clinical and biological research
vol. 18
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33.
Adult hemoglobin synthesis by reticulocytes from the human fetus at midtrimester.
[electronic resource]
by
Hollenberg, M D
Kaback, M M
Kazazian, H H
Producer:
19720202
In:
Science (New York, N.Y.)
vol. 174
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34.
Significant of meconium stained fluid in midtrimester amniocentesis.
[electronic resource]
by
Immken, L
Lee, M
Stewart, R
Kaback, M M
Producer:
19821216
In:
Birth defects original article series
vol. 18
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35.
Diagnosis and excision of an intrapericardial teratoma in an infant.
[electronic resource]
by
White, J J
Kaback, M M
Haller, J A
Producer:
19680710
In:
The Journal of thoracic and cardiovascular surgery
vol. 55
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36.
Cerebroside sulphate (sulphatide) sulphohydrolase: an improved assay method.
[electronic resource]
by
Percy, A K
Farrell, D F
Kaback, M M
Producer:
19720407
In:
Journal of neurochemistry
vol. 19
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37.
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidase.
[electronic resource]
by
Paw, B H
Kaback, M M
Neufeld, E F
Producer:
19890505
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 86
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38.
Metachromatic leukodystrophy: comparison of early-and late-onset forms.
[electronic resource]
by
Percy, A K
Kaback, M M
Herndon, R M
Producer:
19771130
In:
Neurology
vol. 27
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39.
Inherited lipid storage diseases of the central nervous system.
[electronic resource]
by
Percy, A K
Shapiro, L J
Kaback, M M
Producer:
19800324
In:
Current problems in pediatrics
vol. 9
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40.
The American Society of Human Genetics statement on cystic fibrosis screening.
[electronic resource]
by
Caskey, C T
Kaback, M M
Beaudet, A L
Producer:
19900312
In:
American journal of human genetics
vol. 46
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