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The chromosome 22q11.2 deletion syndrome a multidisciplinary approach to diagnosis and treatment /
The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the etiology, prognosis, and recurrence risk associated with the chromosome 22q11.2 deletion syndrome. Leading international contributors cov...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
London, United Kingdom :
Academic Press,
2022.
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000 a 4500 | ||
|---|---|---|---|
| 001 | SCIDIR_on1341985403 | ||
| 003 | OCoLC | ||
| 005 | 20231120010700.0 | ||
| 006 | m o d | ||
| 007 | cr un|---aucuu | ||
| 008 | 220825s2022 enk o 001 0 eng d | ||
| 040 | |a YDX |b eng |c YDX |d OPELS |d N$T |d OCLCF |d OCLCQ |d OCLCO | ||
| 020 | |a 9780128160480 |q (electronic bk.) | ||
| 020 | |a 0128160489 |q (electronic bk.) | ||
| 020 | |z 9780128160473 |q (print) | ||
| 020 | |z 0128160470 |q (print) | ||
| 035 | |a (OCoLC)1341985403 | ||
| 050 | 4 | |a RB155.5 | |
| 082 | 0 | 4 | |a 616/.042 |2 23 |
| 245 | 0 | 4 | |a The chromosome 22q11.2 deletion syndrome |h [electronic resource] : |b a multidisciplinary approach to diagnosis and treatment / |c edited by Donna M. McDonald-McGinn. |
| 260 | |a London, United Kingdom : |b Academic Press, |c 2022. | ||
| 300 | |a 1 online resource | ||
| 520 | |a The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the etiology, prognosis, and recurrence risk associated with the chromosome 22q11.2 deletion syndrome. Leading international contributors cover the background, genetics, testing methods, and pathophysiology of 22q11.2DS, placing emphasis on a strong foundation for multidisciplinary treatment strategies. Written by specialists in every applicable subspecialty, such as, cardiology, immunology, endocrinology, gastroenterology, hematology, ophthalmology, neurology, and psychiatry, among other fields. This book presents an authoritative resource with full color images that enhance concept illustration and aid in real-time decision-making. As 22q11.2 deletion syndrome has become a model for understanding rare and frequent anomalies, numerous medical issues, cognitive and behavioral phenotypes, and later onset conditions, this text will become the go to resource for clinicians, researchers, trainees, and motivated family members, in gaining a full understanding of this complex chromosomal disorder. | ||
| 500 | |a Includes index. | ||
| 588 | 0 | |a Print version record. | |
| 650 | 0 | |a Human chromosome abnormalities. | |
| 650 | 6 | |a Chromosomes humains |x Anomalies. |0 (CaQQLa)201-0035898 | |
| 650 | 7 | |a Human chromosome abnormalities |2 fast |0 (OCoLC)fst00962907 | |
| 700 | 1 | |a McDonald-McGinn, Donna M., |e editor. | |
| 776 | 0 | 8 | |i Print version: |z 0128160470 |z 9780128160473 |w (OCoLC)1111637447 |
| 776 | 0 | 8 | |i Print version: |t Chromosome 22q11.2 deletion syndrome |z 9780128160473 |w (OCoLC)1197812931 |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780128160473 |z Texto completo |