Management of genetic syndromes/
| Corporate Author: | |
|---|---|
| Other Authors: | , |
| Format: | Book |
| Language: | English |
| Published: |
Hoboken, NJ:
Wiley-Liss,
c2005
|
| Edition: | 2η έκδ. |
| Subjects: |
Table of Contents:
- Aarskog syndrome / Roger E. Stevenson
- Achondroplasia / Richard M. Pauli
- Alagille syndrome / Binita M. Kamath and Ian Krantz
- Albinism / Richard A. King and C. Gail Summers
- Angelman syndrome / Charles A. Williams
- Arthrogryposis / Judith G. Hall
- ATR-X / Richard J. Gibbons
- Bardet-Biedl syndrome / Anne M. Slavotinek
- Beckwith-Wiedemann syndrome / Rosanna Weksberg and Cheryl Shuman
- CHARGE association / Christine A. Oley
- Coffin-Lowry syndrome / Alasdair G.W. Hunter
- Cornelia de Lange syndrome / David E. Fitzpatrick and Antonie D. Kline
- Costello syndrome / Angela E. Lin, Karen W. Gripp and Bronwyn Kerr
- Craniosynostosis / Karen W. Gripp and Elaine H. Zackai
- Denys-Drash syndrome / Carol L. Clericuzio
- Down syndrome / Alasdair G.W. Hunter
- Ehlers-Danlos syndrome / Richard J. Wenstrup and Leah B. Hoechstetter
- Fetal alcohol syndrome / Albert E. Chudley and Sally E. Longstaffe
- Fetal anticonvulsants / Renata C. Gallagher, Kerry Kingham and H. Eugene Hoyme
- Fragile X syndrome / Randi J. Hagerman
- Gorlin syndrome (nevoid basal cell carcinoma syndrome) / Peter Farndon
- Hereditary haemorrhagic telangiectasia / Mary E.M. Porteous
- Holoprosencephaly / Andrea L. Gropman and Maximilian Muenke
- Incontinetia pigmenti / Dian Donnai
- Kabuki syndrome / Louanne Hudgins
- Klinefelter syndrome / Joe Leigh Simpson .. [και ά.]
- Marfan syndrome / Iris Schrijver, Deborah M. Alcorn and Uta Francke
- Myotonic dystrophy / Christine E.M. deDie Smulders, Frans G.I. Jennekens and Chris J. H"weler
- Neurofibromatosis type 1 / David Viskochil
- Noonan syndrome / Judith E. Allanson
- Oculo-auriculo-vertebral spectrum / Robert J. Gorlin
- Osteogenesis imperfecta / Joan C, Marin, Anne Letocha and Edith J. Chernoff
- Pallister-Hall and Greig cephalopolysyndactyly syndrome / Leslie G. Biesecker
- Prader-Willi syndrome / Suzanne B. Cassidy
- Proteus syndrome / Leslie G. Biesecker
- Rett syndrome / Eric E. Smeets and Connie T.R.M. Schrander-Stumpel
- Robin sequence / Robert J. Shprintzen
- Rubinstein-Taybi syndrome / Raoul C.M. Hennekam
- Russell-Silver syndrome / Howard M. Saal
- Smith-Lemli-Opitz syndrome / Christopher Cunniff and Theresa A. Grebe
- Smith-Magenis syndrome / Ann C.M. Smith
- Sotos syndrome / Trevor R.P. Cole
- Stickler syndrome / Clair Francomano, Douglas J. Wilkin and Ruth M. Liberfarb
- Terminal 22q- / Mary C. Phelan, Gail A. Stapleton and R. Curtis Rogers
- Treacher-Collins syndrome / Marilyn C. Jones
- Trisomy 13 and 18 syndromes / John C. Carey
- Tuberous sclerosis / John R.W. Yates
- Turner syndrome / Virginia P. Sybert
- VATER syndrome / Bryan D. Hall
- Velo-Cario-facial syndrome / Robert J. Shprintzen
- Von Hippel Lindau syndrome / R. Neil Schimke and Debra L. Collins
- WAGR syndrome / Carol L. Clericuzio
- Williams syndrome / Colleen A. Morris
- Wolf-Hirschhorn / Agatino Battaglia.