1.

Record Nr.

UNINA9910465337303321

Titolo

Epstein's inborn errors of development : the molecular basis of clinical disorders of morphogenesis / / edited by Robert P. Erickson, Anthony Wynshaw-Boris

Pubbl/distr/stampa

New York, New York : , : Oxford University Press, , 2016

©2016

ISBN

0-19-021353-1

0-19-027542-1

Edizione

[Third edition.]

Descrizione fisica

1 online resource (1553 p.)

Collana

Oxford Monographs on Medical Genetics

Disciplina

616.042

Soggetti

Genetic disorders

Developmental disabilities - Genetic aspects

Genetic disorders in children

Electronic books.

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Description based upon print version of record.

Nota di bibliografia

Includes bibliographical references at the end of each chapters and index.

Nota di contenuto

4. Human Genomics and Human Development                                              II. Patterns of Development                                  ; 5. Development of Left-.Right Asymmetry                                              ; 6. Neural Crest Formation and Craniofacial Development                                                             ; 7. Development of the Nervous System                                           ; 8. Development of the Eye                                ; 9. Development of the Ear

10. Molecular Regulation of Cardiogenesis                                                11. Update on the Development of the Vascular System and Its Sporadic Disorders                                                                                      ; 12. Muscle and Somite Development                                        ; 13. The Development of Bone and Cartilage                                                ; 14. Limb Development                           ; 15. The Sex-.Determination Pathway

Sommario/riassunto

Epstein's Inborn Errors of Development provides essays on pathways of development and thoughtful reviews of dysmorphic syndromes for which the causative gene has been identified. It is a top-to-bottom



revision of the landmark text that both revolutionized and accelerated the field of human genetics.