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1

Fetal Cell Workshop (11th 2000 Basel, Switzerland). Fetal cells and fetal DNA in maternal blood: New developments for a new millennium : 11th Fetal Cell Workshop, Basel, April 15, 2000. Edited by Hahn Sinuhe and Holzgreve Wolfgang. Basel: Karger, 2001.

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2

A, Cohen Shara B., ed. Cord blood characteristics: Role in stem cell transplantation. London: Dunitz, 2000.

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3

Arthur, Ann V. Analysis of fetal globin gene expression in Kuwaitis with sickle cell disease. [New Haven: s.n.], 1990.

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4

1943-, Simpson Joe Leigh, Elias Sherman, and New York Academy of Sciences., eds. Fetal cells in maternal blood: Prospects for noninvasive prenatal diagnosis. New York: New York Academy of Sciences, 1994.

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5

Magin, Angela Susanne. Humane Primärzellen als Feederzellen für die Kokultur mit hämatopoetischen Stammzellen aus Nabelschnurblut. Jülich: Forschungszentrum Jülich, Zentralbibliothek, 2006.

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6

Vinnedge, Debra L. Aborted fetal cell line vaccines and the Catholic family: A moral perspective. Largo, Fla: Children of God for life, 2003.

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7

Wolfgang, Holzgreve, and Lessl M. 1966-, eds. Stem cells from cord blood, in utero stem cell development, and transportation-inclusive gene therapy /cW. Holzgreve, M. Lessl, editors. New York: Springer, 2001.

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8

Frontiers in cord blood science. London: Springer, 2009.

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9

1955-, Freeman Thomas B., and Widner Hakan, eds. Cell transplantation for neurological disorders: Toward reconstruction of the human central nervous system. Totowa, N.J: Humana Press, 1998.

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10

United, States Congress Senate Committee on Health Education Labor and Pensions. Stem Cell Therapeutic and Research Act of 2005: Report (to accompany S. 1317). [Washington, D.C: U.S. G.P.O., 2005.

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11

Stem Cell Therapeutic and Research Act of 2005: Report (to accompany S. 1317). [Washington, D.C: U.S. G.P.O., 2005.

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12

Basic concepts in embryology: A student's survival guide. New York: McGraw-Hill, Health Professions Division, 1998.

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13

Sanberg, Paul R. Cell transplantation for Huntington's disease. Austin: R.G. Landes, 1994.

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14

Sanberg, Paul R. Cell transplantation for Huntington's disease. Austin: R.G. Landes, 1994.

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15

Loke, Y. W. Human implantation: Cell biology and immunology. Cambridge: Cambridge University Press, 1995.

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16

Smirnov, V. N. Therapeutic potential of umbilical cord blood cells for the treatment of nonhematological diseases. Moscow: Kollektiv Avtorov, 2011.

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17

C, Azmitia Efrain, Björklund Anders 1945-, and New York Academy of Sciences., eds. Cell and tissue transplantation into the adult brain. New York, N.Y: New York Academy of Sciences, 1987.

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18

E, Broxmeyer Hal, ed. Cellular characteristics of cord blood and cord blood transplantation. Bethesda, Md: AABB Press, 1998.

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19

Broxmeyer, Hal E. Cord blood: Biology, transplantation, banking, and regulation. Bethesda, Md: AABB Press, 2011.

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20

Klaus, Unsicker, and Krieglstein Kerstin, eds. Cell signaling and growth factors in development: From molecules to organogenesis. Weinheim: Wiley-VCH, 2006.

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21

G, Payne Anthony, ed. Umbilical-cord stem-cell therapy: The gift of healing from healthy newborns. Laguna Beach, CA: Basic Health Publications, 2006.

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22

Stem Cell Therapeutic and Research Reauthorization Act of 2010: Report (to accompany H.R. 6081) (including cost estimate of the Congressional Budget Office). Washington, D.C: U.S. G.P.O., 2010.

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23

Institute of Medicine (U.S.). Committee on Establishing a National Cord Blood Stem Cell Bank Program. Cord blood: Establishing a national hematopoietic stem cell bank program. Edited by Meyer Emily Ann, Hanna Kathi E, and Gebbie Kristine M. Washington, D.C: National Academies Press, 2005.

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24

Bowes, Richard. Feral cell. New York: Warner Books, 1987.

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25

deF, Webster Henry, ed. The early development of the neopallial wall and area choroidea in fetal rats: A light and electron microscopic study. Berlin: Springer-Verlag, 1991.

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26

Veillette, Christian J. H. Role of endothelin-1 in regulation of osteoblast differentiation and vascular endothelial growth factor-A in cell populations from fetal rat calvaria. Ottawa: National Library of Canada, 2002.

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27

Fauza, Dario O., and Mahmud Bani, eds. Fetal Stem Cells in Regenerative Medicine. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3483-6.

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28

L, Touraine J., Gale Robert Peter, and Kochupillai Vinod, eds. Fetal liver transplantation. Dordrecht: Nijhoff, 1987.

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29

Riccio, Veronica Del. Stretch-induced apoptosis in fetal lung cells. Ottawa: National Library of Canada, 2003.

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30

Fetal therapy: Scientific basis and critical appraisal of clinical benefits. Cambridge: Cambridge University Press, 2012.

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31

Lee, Yeojin. Extrinsic regulation of Hematopoietic Stem Cells in the fetal liver. [New York, N.Y.?]: [publisher not identified], 2021.

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32

1956-, Lanza R. P., ed. Handbook of stem cells. Boston, MA: Elsevier Academic, 2004.

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33

Lanza, R. P. Handbook of stem cells. London: Elsevier/AP, 2013.

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34

Rader, William. Fetal Stem Cell Miracle. Phoenix Books, Inc., 2009.

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35

Fetal cell transplantation: Guidance for nurses. London: Royal College of Nursing, 1992.

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36

Lam, Kong-Peng. Fetal- and adult-type B cell development. 1994.

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37

Song, Priscilla. Biomedical Odysseys: Fetal Cell Experiments from Cyberspace to China. Princeton University Press, 2017.

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38

Song, Priscilla. Biomedical Odysseys: Fetal Cell Experiments from Cyberspace to China. Princeton University Press, 2017.

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39

Song, Priscilla. Biomedical Odysseys - Fetal Cell Experiments from Cyberspace to China. Princeton University Press, 2017.

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40

Ilic, Dusko. Stem Cell Banking. Springer, 2016.

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41

Ilic, Dusko. Stem Cell Banking. Springer, 2014.

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42

Ilic, Dusko. Stem Cell Banking. Springer London, Limited, 2014.

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43

Cord Blood Characteristics: Role in Stem Cell Transplantation. Informa Healthcare, 2000.

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44

Hahn, Sinuhe. Fetal Cells and Fetal DNA in Maternal Blood: New Developments for a New Millennium. Edited by Sinuhe Hahn. Karger, 2001.

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45

Provan, Drew, Trevor Baglin, Inderjeet Dokal, and Johannes de Vos. Red cell disorders. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199683307.003.0002.

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The peripheral blood film in anaemias - Anaemia in renal disease - Anaemia in endocrine disease - Anaemia in joint disease - Anaemia in gastrointestinal disease - Anaemia in liver disease - Iron (Fe) deficiency anaemia - Vitamin B12 deficiency - Folate deficiency - Other causes of megaloblastic anaemia - Anaemia in other deficiency states - Haemolytic syndromes - Genetic control of haemoglobin production - Sickling disorders - HbS—sickle-modifying therapies - Sickle cell trait (HbAS) - Other sickling disorders - Other haemoglobinopathies - Unstable haemoglobins - Thalassaemias - α thalassaemia - β thalassaemia - Other thalassaemias - Hereditary persistence of fetal haemoglobin - Hb patterns in haemoglobin disorders - Non-immune haemolysis - Hereditary spherocytosis - Hereditary elliptocytosis - Glucose-6-phosphate dehydrogenase (G6PD) deficiency - Pyruvate kinase deficiency - Other red cell enzymopathies - Drug-induced haemolytic anaemia - Methaemoglobinaemia - Microangiopathic haemolytic anaemia - Acanthocytosis - Autoimmune haemolytic anaemia - Cold haemagglutinin disease - Leucoerythroblastic anaemia - Aplastic anaemia - Paroxysmal nocturnal haemoglobinuria - Pure red cell aplasia - Iron (Fe) overload - Transfusion haemosiderosis
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46

Provan, Drew, Trevor Baglin, Inderjeet Dokal, Johannes de Vos, Banu Kaya, and Angela Theodoulou. Red cell disorders. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199683307.003.0002_update_001.

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The peripheral blood film in anaemias - Anaemia in renal disease - Anaemia in endocrine disease - Anaemia in joint disease - Anaemia in gastrointestinal disease - Anaemia in liver disease - Iron (Fe) deficiency anaemia - Vitamin B12 deficiency - Folate deficiency - Other causes of megaloblastic anaemia - Anaemia in other deficiency states - Haemolytic syndromes - Genetic control of haemoglobin production - Sickling disorders - HbS—sickle-modifying therapies - Sickle cell trait (HbAS) - Other sickling disorders - Other haemoglobinopathies - Unstable haemoglobins - Thalassaemias - α‎ thalassaemia - β‎ thalassaemia - Other thalassaemias - Hereditary persistence of fetal haemoglobin - Hb patterns in haemoglobin disorders - Non-immune haemolysis - Hereditary spherocytosis - Hereditary elliptocytosis - Glucose-6-phosphate dehydrogenase (G6PD) deficiency - Pyruvate kinase deficiency - Other red cell enzymopathies - Drug-induced haemolytic anaemia - Methaemoglobinaemia - Microangiopathic haemolytic anaemia - Acanthocytosis - Autoimmune haemolytic anaemia - Cold haemagglutinin disease - Leucoerythroblastic anaemia - Aplastic anaemia - Paroxysmal nocturnal haemoglobinuria - Pure red cell aplasia - Iron (Fe) overload - Transfusion haemosiderosis
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47

Broxmeyer, Hal E. Cord Blood: Biology, Immunology, Banking, and Clinical Transplantation. Not Avail, 2004.

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48

Broxmeyer, Hal E. Cord Blood: Biology, Immunology, And Clinical Transplantation. American Association of Blood Banks (AABB), 2004.

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49

Lopez, Cecilia Ang. Agents enhancing oncogene-induced transformation of cultured rodent fibroblasts: Purification of a fetal calf serum. 1987.

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50

Lopez-Arvizu, Carmen, Carmel Bogle, and Harolyn M. E. Belcher. Neurobiology of Fetal Alcohol Spectrum Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0179.

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Prenatal exposure to ethanol can result in a wide range of clinical presentations that are grouped under the term “Fetal Alcohol Spectrum Disorders” (FASD). The direct cellular teratogenic effects of ethanol on fetal neurodevelopment include damage to cell survival, proliferation, and migration mechanisms. Dysregulation of neurotransmission and alteration of genetic transcription have also been implicated in the neurotoxic effects of prenatal ethanol exposure. These deleterious events lead to brain volume reduction, corpus callosum dysgenesis, cerebellar, and other neuroanatomical anomalies that have been observed in individuals with FASD. Beyond direct ethanol-induced insults, the impact that ethanol has on maternal nutrition, metabolism, hormonal regulation, and placental physiology also adversely effects fetal development. The complex interactions between numerous neurobiological and psychosocial mechanisms that hinder optimal fetal neurodevelopment are reflected by the heterogeneous clinical presentation of FASD, including impaired growth, dysmorphic facial features, and cognitive and behavioral disorders.
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