مکتبة رقمیه للعلوم الطبيه
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  2. Details for: International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.
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International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. [electronic resource]

By:
  • Boycott, Kym M
Contributor(s):
  • Rath, Ana
  • Chong, Jessica X
  • Hartley, Taila
  • Alkuraya, Fowzan S
  • Baynam, Gareth
  • Brookes, Anthony J
  • Brudno, Michael
  • Carracedo, Angel
  • den Dunnen, Johan T
  • Dyke, Stephanie O M
  • Estivill, Xavier
  • Goldblatt, Jack
  • Gonthier, Catherine
  • Groft, Stephen C
  • Gut, Ivo
  • Hamosh, Ada
  • Hieter, Philip
  • Höhn, Sophie
  • Hurles, Matthew E
  • Kaufmann, Petra
  • Knoppers, Bartha M
  • Krischer, Jeffrey P
  • Macek, Milan
  • Matthijs, Gert
  • Olry, Annie
  • Parker, Samantha
  • Paschall, Justin
  • Philippakis, Anthony A
  • Rehm, Heidi L
  • Robinson, Peter N
  • Sham, Pak-Chung
  • Stefanov, Rumen
  • Taruscio, Domenica
  • Unni, Divya
  • Vanstone, Megan R
  • Zhang, Feng
  • Brunner, Han
  • Bamshad, Michael J
  • Lochmüller, Hanns
Producer: 20170727Description: 695-705 p. digitalISSN:
  • 1537-6605
Subject(s):
  • Databases, Factual
  • Exome
  • Genome, Human
  • Humans
  • International Cooperation
  • Rare Diseases -- diagnosis
Online resources:
  • Available from publisher's website
In: American journal of human genetics vol. 100
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Publication Type: Journal Article

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International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.

APA

Boycott K. M., Rath A., Chong J. X., Hartley T., Alkuraya F. S., Baynam G., Brookes A. J., Brudno M., Carracedo A., den Dunnen J. T., Dyke S. O. M., Estivill X., Goldblatt J., Gonthier C., Groft S. C., Gut I., Hamosh A., Hieter P., Höhn S., Hurles M. E., Kaufmann P., Knoppers B. M., Krischer J. P., Macek M., Matthijs G., Olry A., Parker S., Paschall J., Philippakis A. A., Rehm H. L., Robinson P. N., Sham P., Stefanov R., Taruscio D., Unni D., Vanstone M. R., Zhang F., Brunner H., Bamshad M. J. & Lochmüller H. (20170727). International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. : American journal of human genetics.

Chicago

Boycott Kym M, Rath Ana, Chong Jessica X, Hartley Taila, Alkuraya Fowzan S, Baynam Gareth, Brookes Anthony J, Brudno Michael, Carracedo Angel, den Dunnen Johan T, Dyke Stephanie O M, Estivill Xavier, Goldblatt Jack, Gonthier Catherine, Groft Stephen C, Gut Ivo, Hamosh Ada, Hieter Philip, Höhn Sophie, Hurles Matthew E, Kaufmann Petra, Knoppers Bartha M, Krischer Jeffrey P, Macek Milan, Matthijs Gert, Olry Annie, Parker Samantha, Paschall Justin, Philippakis Anthony A, Rehm Heidi L, Robinson Peter N, Sham Pak-Chung, Stefanov Rumen, Taruscio Domenica, Unni Divya, Vanstone Megan R, Zhang Feng, Brunner Han, Bamshad Michael J and Lochmüller Hanns. 20170727. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. : American journal of human genetics.

Harvard

Boycott K. M., Rath A., Chong J. X., Hartley T., Alkuraya F. S., Baynam G., Brookes A. J., Brudno M., Carracedo A., den Dunnen J. T., Dyke S. O. M., Estivill X., Goldblatt J., Gonthier C., Groft S. C., Gut I., Hamosh A., Hieter P., Höhn S., Hurles M. E., Kaufmann P., Knoppers B. M., Krischer J. P., Macek M., Matthijs G., Olry A., Parker S., Paschall J., Philippakis A. A., Rehm H. L., Robinson P. N., Sham P., Stefanov R., Taruscio D., Unni D., Vanstone M. R., Zhang F., Brunner H., Bamshad M. J. and Lochmüller H. (20170727). International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. : American journal of human genetics.

MLA

Boycott Kym M, Rath Ana, Chong Jessica X, Hartley Taila, Alkuraya Fowzan S, Baynam Gareth, Brookes Anthony J, Brudno Michael, Carracedo Angel, den Dunnen Johan T, Dyke Stephanie O M, Estivill Xavier, Goldblatt Jack, Gonthier Catherine, Groft Stephen C, Gut Ivo, Hamosh Ada, Hieter Philip, Höhn Sophie, Hurles Matthew E, Kaufmann Petra, Knoppers Bartha M, Krischer Jeffrey P, Macek Milan, Matthijs Gert, Olry Annie, Parker Samantha, Paschall Justin, Philippakis Anthony A, Rehm Heidi L, Robinson Peter N, Sham Pak-Chung, Stefanov Rumen, Taruscio Domenica, Unni Divya, Vanstone Megan R, Zhang Feng, Brunner Han, Bamshad Michael J and Lochmüller Hanns. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. : American journal of human genetics. 20170727.

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