Van Went J L (25 results)

Condition: New.

Paperback or Softback. Condition: New. Early Diagnosis and Prevention of Genetic Diseases. Book.

Pictorial hard covers. Condition: Fine. No Jacket. 1st edition. Little used. Weight: 1.0 Language: English.

Condition: New.

Condition: As New. Unread book in perfect condition.

of Petunia Hybrida (S. A. Acta Bot. Neerl. 25, 5) 1976. S. 381 - 383. m. zahlr. Abb. br. -2) -Sonderabdruck-.

translocation studies (S. A. Acta Bot. Neerl. 24, 1) 1975. S. 1 - 6. m. zahlr. Abb. br. -2) -Sonderabdruck-.

(S. A. Acta Bot. Neerl. 19, 3) 1970. S. 313 - 322. m. zahlr. Abb. br. -2) -Sonderabdruck-.

(S. A. Acta Bot. Neerl. 19, 4) 1970. S. 468 - 474. m. zahlr. Abb. br. -2) -Sonderabdruck-.

(S. A. Planta 133) 1976. S. 35 - 40. gr8. m. zahlr. Abb. br. -2) -Sonderabdruck-.

(S. A. Acta Bot. Neerld. 19, 2) 1970. S. 121 - 132. m. zahlr. Abb. br. -2) -Sonderabdruck-.

Condition: New. In.

PF. Condition: New.

Condition: New.

Condition: As New. Unread book in perfect condition.

Condition: New. pp. 172.

Paperback. Condition: Brand New. 172 pages. 9.02x5.98x0.39 inches. In Stock.

Soft cover. figs, paperbound 0.0.

Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - The present volume of the Boerhaave series intends to be a reflexion of our present knowledge in the expanding field of early diagnosis and prevention of inherited disorders. Early diagnosis can mean detection of a carrier state in one or both potential parents, detection of a specific inherited disease in a previously born child or during a pregnancy at risk, or during various stages of the life of an already born individual. The first chapters will discuss inherited disorders manifesting later in life. In Huntington's Chorea detection may be possible from the age of 20 or 30 onwards, while in myotonic dystrophy it will be seen that detection may be possible soon after birth. Retinoblastoma serves as example of a disease manifesting in early infancy and which is partially treatable by surgical intervention. The same early onset does occur in phenylketonuria and cystic fibrosis. Both diseases provide examples of the possibilities of population screening, while in phenylketonuria an eminently succesful treatment is found in a restricted diet. For the usually early manifesting sphingolipidoses no treatment exists as yet, but enzyme treatment might in the near future become a reality. Spina bifida and anencephaly are not simple inherited Mendelian dis orders but they are discussed in this volume because prevention is possible by antenatal diagnosis and subsequent interruption of the pregnancy if re quested by the future parents. Further views on antenatal diagnosis notably in inborn errors of metabolism are presented in a following chapter.…

Condition: new. Questo è un articolo print on demand.

Condition: New. Print on Demand pp. 172 23:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on White w/Gloss Lam.

Condition: New. PRINT ON DEMAND pp. 172.

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. The present volume of the Boerhaave series intends to be a reflexion of our present knowledge in the expanding field of early diagnosis and prevention of inherited disorders. Early diagnosis can mean detection of a carrier state in one or both potential par.…

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The present volume of the Boerhaave series intends to be a reflexion of our present knowledge in the expanding field of early diagnosis and prevention of inherited disorders. Early diagnosis can mean detection of a carrier state in one or both potential parents, detection of a specific inherited disease in a previously born child or during a pregnancy at risk, or during various stages of the life of an already born individual. The first chapters will discuss inherited disorders manifesting later in life. In Huntington's Chorea detection may be possible from the age of 20 or 30 onwards, while in myotonic dystrophy it will be seen that detection may be possible soon after birth. Retinoblastoma serves as example of a disease manifesting in early infancy and which is partially treatable by surgical intervention. The same early onset does occur in phenylketonuria and cystic fibrosis. Both diseases provide examples of the possibilities of population screening, while in phenylketonuria an eminently succesful treatment is found in a restricted diet. For the usually early manifesting sphingolipidoses no treatment exists as yet, but enzyme treatment might in the near future become a reality. Spina bifida and anencephaly are not simple inherited Mendelian dis orders but they are discussed in this volume because prevention is possible by antenatal diagnosis and subsequent interruption of the pregnancy if re quested by the future parents. Further views on antenatal diagnosis notably in inborn errors of metabolism are presented in a following chapter. 172 pp. Englisch.…

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The present volume of the Boerhaave series intends to be a reflexion of our present knowledge in the expanding field of early diagnosis and prevention of inherited disorders. Early diagnosis can mean detection of a carrier state in one or both potential parents, detection of a specific inherited disease in a previously born child or during a pregnancy at risk, or during various stages of the life of an already born individual. The first chapters will discuss inherited disorders manifesting later in life. In Huntington's Chorea detection may be possible from the age of 20 or 30 onwards, while in myotonic dystrophy it will be seen that detection may be possible soon after birth. Retinoblastoma serves as example of a disease manifesting in early infancy and which is partially treatable by surgical intervention. The same early onset does occur in phenylketonuria and cystic fibrosis. Both diseases provide examples of the possibilities of population screening, while in phenylketonuria an eminently succesful treatment is found in a restricted diet. For the usually early manifesting sphingolipidoses no treatment exists as yet, but enzyme treatment might in the near future become a reality. Spina bifida and anencephaly are not simple inherited Mendelian dis orders but they are discussed in this volume because prevention is possible by antenatal diagnosis and subsequent interruption of the pregnancy if re quested by the future parents. Further views on antenatal diagnosis notably in inborn errors of metabolism are presented in a following chapter.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 172 pp. Englisch.…