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  • Kaback, Michael M., M.D., editor

    Published by W.B. Saunders (1978) Philadelphia, 1978

    Seller: Prairie Archives, Springfield, IL, U.S.A.

    Association Member: MWABA

    Seller rating 5 out of 5 stars 5-star rating, Learn more about seller ratings

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    US$ 9.00

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    Quantity: 1 available

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    Good plus or better, light general wear, slightly cocked spine Cloth.

  • Kaback, Michael M. (MD), Editor

    Published by Alan R. Liss, Inc., NY, 1977

    Seller: UHR Books, Hollis Center, ME, U.S.A.

    Association Member: MABA

    Seller rating 5 out of 5 stars 5-star rating, Learn more about seller ratings

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    First Edition

    US$ 19.54

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    Hardcover. Condition: Very Good. No Jacket. First Edition. "Based on the first international conference on Tay-Sachs Disease" held in Palm Springs, California in 1975. Covers research on the screening and prevention of TSD, religious perspectives, the TSD Gene, prospects for therapy, genetic variants of TSD, screening methods and quality control, prenatal diagnosis, carrier screening and genetic counseling, psychosocial considerations, and more. Several contributing authors. Ex-Library.

  • Kaback, Michael M. (Guest Editor)

    Language: English

    Published by W.B. Saunders, Philadelphia, PA, 1978

    Seller: 100POCKETS, Berkeley, CA, U.S.A.

    Seller rating 4 out of 5 stars 4-star rating, Learn more about seller ratings

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    US$ 28.75

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    Hardcover. Condition: Near Fine. Volume 25, Number 3. Text/BRAND NEW & Bright. Vintage 1978 pediatric medical symposium publication. Gilt embossed green linen boards/NF, showing light discoloration. PO name to fEP. Quarterly publication. This issue contains: 1, Medical Genetics: An Overview (Michael M. Kaback); 2, Newborn Screening for Inborn Errors of Metabolism; 3, Neonatal Thyroid Screening; 4, Genetic-Metabolic Considerations in the Sick Neonate; 5, Neonatal Dwarfism; 6, Craniofacial Malformations; 7, Recent Cytogenetic Advances & Implications for Pediatric Practice; 8, Hereditary Considerations in Common Disorders; 9, Diagnosis, Carrier Detection, & Genetic Counseling in the Muscular Dystrophies; 10, Heritable Disorders of Connective Tissue: Ehlers-Danlos Syndrome; 11, Prenatal Diagnosis of Hereditary Disorders; 12, Neural Tube Defects; 13, Prenatal Diagnosis of Hemoglobinopathies; and, 14, Crisis Conseling: The Newborn Infant with a Chromosomal Anomaly.