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  2. Details for: Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.
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Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. [electronic resource]

By:
  • Stolerman, Elliot S
Contributor(s):
  • Francisco, Elizabeth
  • Stallworth, Jennifer L
  • Jones, Julie R
  • Monaghan, Kristin G
  • Keller-Ramey, Jennifer
  • Person, Richard
  • Wentzensen, Ingrid M
  • McWalter, Kirsty
  • Keren, Boris
  • Heron, Benedicte
  • Nava, Caroline
  • Heron, Delphine
  • Kim, Katherine
  • Burton, Barbara
  • Al-Musafri, Fatima
  • O'Grady, Lauren
  • Sahai, Inderneel
  • Escobar, Luis F
  • Meuwissen, Marije
  • Reyniers, Edwin
  • Kooy, Frank
  • Lacassie, Yves
  • Gunay-Aygun, Meral
  • Schatz, Krista Sondergaard
  • Hochstenbach, Ron
  • Zwijnenburg, Petra J G
  • Waisfisz, Quinten
  • van Slegtenhorst, Marjon
  • Mancini, Grazia M S
  • Louie, Raymond J
Producer: 20200708Description: 1276-1286 p. digitalISSN:
  • 1552-4833
Subject(s):
  • Adolescent
  • Child, Preschool
  • Cohort Studies
  • Female
  • Genetic Variation
  • Humans
  • Jumonji Domain-Containing Histone Demethylases -- genetics
  • Male
  • Neurodevelopmental Disorders -- genetics
Online resources:
  • Available from publisher's website
In: American journal of medical genetics. Part A vol. 179
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Publication Type: Journal Article

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Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.

APA

Stolerman E. S., Francisco E., Stallworth J. L., Jones J. R., Monaghan K. G., Keller-Ramey J., Person R., Wentzensen I. M., McWalter K., Keren B., Heron B., Nava C., Heron D., Kim K., Burton B., Al-Musafri F., O'Grady L., Sahai I., Escobar L. F., Meuwissen M., Reyniers E., Kooy F., Lacassie Y., Gunay-Aygun M., Schatz K. S., Hochstenbach R., Zwijnenburg P. J. G., Waisfisz Q., van Slegtenhorst M., Mancini G. M. S. & Louie R. J. (20200708). Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. : American journal of medical genetics. Part A.

Chicago

Stolerman Elliot S, Francisco Elizabeth, Stallworth Jennifer L, Jones Julie R, Monaghan Kristin G, Keller-Ramey Jennifer, Person Richard, Wentzensen Ingrid M, McWalter Kirsty, Keren Boris, Heron Benedicte, Nava Caroline, Heron Delphine, Kim Katherine, Burton Barbara, Al-Musafri Fatima, O'Grady Lauren, Sahai Inderneel, Escobar Luis F, Meuwissen Marije, Reyniers Edwin, Kooy Frank, Lacassie Yves, Gunay-Aygun Meral, Schatz Krista Sondergaard, Hochstenbach Ron, Zwijnenburg Petra J G, Waisfisz Quinten, van Slegtenhorst Marjon, Mancini Grazia M S and Louie Raymond J. 20200708. Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. : American journal of medical genetics. Part A.

Harvard

Stolerman E. S., Francisco E., Stallworth J. L., Jones J. R., Monaghan K. G., Keller-Ramey J., Person R., Wentzensen I. M., McWalter K., Keren B., Heron B., Nava C., Heron D., Kim K., Burton B., Al-Musafri F., O'Grady L., Sahai I., Escobar L. F., Meuwissen M., Reyniers E., Kooy F., Lacassie Y., Gunay-Aygun M., Schatz K. S., Hochstenbach R., Zwijnenburg P. J. G., Waisfisz Q., van Slegtenhorst M., Mancini G. M. S. and Louie R. J. (20200708). Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. : American journal of medical genetics. Part A.

MLA

Stolerman Elliot S, Francisco Elizabeth, Stallworth Jennifer L, Jones Julie R, Monaghan Kristin G, Keller-Ramey Jennifer, Person Richard, Wentzensen Ingrid M, McWalter Kirsty, Keren Boris, Heron Benedicte, Nava Caroline, Heron Delphine, Kim Katherine, Burton Barbara, Al-Musafri Fatima, O'Grady Lauren, Sahai Inderneel, Escobar Luis F, Meuwissen Marije, Reyniers Edwin, Kooy Frank, Lacassie Yves, Gunay-Aygun Meral, Schatz Krista Sondergaard, Hochstenbach Ron, Zwijnenburg Petra J G, Waisfisz Quinten, van Slegtenhorst Marjon, Mancini Grazia M S and Louie Raymond J. Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. : American journal of medical genetics. Part A. 20200708.

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