Kaback michael editor (3 risultati)
Editore: W.B. Saunders (1978) Philadelphia 1978
- Rilegato
Da: Prairie Archives, Springfield, IL, U.S.A.Prairie Archives
Contatta il venditoreVenditore con 4 stelleMembro dell’associazione: MWABA
Condizione: Usato
EUR 8,16
EUR 4,62 spedizioneSpedito in U.S.A.Quantità: 1 disponibili
Good plus or better, light general wear, slightly cocked spine Cloth.
Editore: Alan R. Liss, Inc., NY 1977
- Rilegato
- Prima edizione
Da: UHR Books, Hollis Center, ME, U.S.A.UHR Books
Contatta il venditoreVenditore con 5 stelleMembro dell’associazione: MABA
Condizione: Usato - Molto buono
EUR 17,73
EUR 3,49 spedizioneSpedito in U.S.A.Quantità: 1 disponibili
Hardcover. Condizione: 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 a…nd quality control, prenatal diagnosis, carrier screening and genetic counseling, psychosocial considerations, and more. Several contributing authors. Ex-Library.
Lingua: Inglese
Editore: W.B. Saunders, Philadelphia, PA 1978
- Rilegato
Da: 100POCKETS, Berkeley, CA, U.S.A.100POCKETS
Contatta il venditoreVenditore con 4 stelleCondizione: Usato - Quasi ottimo
EUR 26,08
EUR 6,61 spedizioneSpedito in U.S.A.Quantità: 1 disponibili
Hardcover. Condizione: Near Fine. Condizione sovraccoperta: None as Issued. 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 Over…view (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.