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Search Results - Sandstrom, Mary McH
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EXTREME VARIANT OF ENLARGED HETEROCHROMATIN REGION ON CHROMOSOME 9Q IN A NORMAL CHILD AND MULTIPLE FAMILY MEMBERS
by
Steffensen, Thora S.
,
Gilbert-Barness, Enid
,
McH. Sandstrom, Mary
,
Bell, John R.
,
Bryan, Jenny
,
Sutcliffe, Maxine J.
Published in
Fetal and pediatric pathology
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Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases
by
Weremowicz, Stanislawa
,
Sandstrom, Deborah J.
,
Morton, Cynthia C.
,
Niedzwiecki, Catherine A.
,
Sandstrom, Mary McH
,
Bieber, Frederick R.
Published in
Prenatal diagnosis
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Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21
by
Lee, Charles
,
Fowler, Darren J.
,
Lemyre, Emmanuelle
,
Sandstrom, Mary McH
,
Holmes, Lewis B.
,
Morton, Cynthia C.
Published in
American journal of medical genetics
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American Journal Of Medical Genetics
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Fetal And Pediatric Pathology
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Prenatal Diagnosis
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Female
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Humans
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Karyotyping
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Life Sciences & Biomedicine
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Prenatal Diagnosis
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Trisomy
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Ultrasonography, Prenatal
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Abnormalities, Multiple - Diagnosis
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Abnormalities, Multiple - Diagnostic Imaging
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Abnormalities, Multiple - Genetics
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Amniotic Fluid
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Science Citation Index Expanded (Web Of Science)
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Wiley-Blackwell Journals
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Taylor And Francis:jisc Collections:taylor And Francis Read And Publish Agreement 2024-2025:Medical Collection (Reading List)
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