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GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6Ψ) mutation

Publication ,  Conference
Chatterjee, S; Rose, SJ; Mushtaq, T; Cottrell, E; Maharaj, AV; Williams, J; Savage, MO; Metherell, LA; Storr, HL
Published in: HORMONE RESEARCH IN PAEDIATRICS
2019

Duke Scholars

Published In

HORMONE RESEARCH IN PAEDIATRICS

EISSN

1663-2826

ISSN

1663-2818

Publication Date

2019

Volume

91

Start / End Page

111 / 111

Related Subject Headings

  • Endocrinology & Metabolism
  • 3215 Reproductive medicine
  • 3213 Paediatrics
  • 3202 Clinical sciences
  • 1114 Paediatrics and Reproductive Medicine
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Chatterjee, S., Rose, S. J., Mushtaq, T., Cottrell, E., Maharaj, A. V., Williams, J., … Storr, H. L. (2019). GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6Ψ) mutation. In HORMONE RESEARCH IN PAEDIATRICS (Vol. 91, pp. 111–111).
Chatterjee, Sumana, Steven J. Rose, Talat Mushtaq, Emily Cottrell, Avinaash V. Maharaj, Jack Williams, Martin O. Savage, Loiuse A. Metherell, and Helen L. Storr. “GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6Ψ) mutation.” In HORMONE RESEARCH IN PAEDIATRICS, 91:111–111, 2019.
Chatterjee S, Rose SJ, Mushtaq T, Cottrell E, Maharaj AV, Williams J, et al. GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6Ψ) mutation. In: HORMONE RESEARCH IN PAEDIATRICS. 2019. p. 111–111.
Chatterjee, Sumana, et al. “GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6Ψ) mutation.” HORMONE RESEARCH IN PAEDIATRICS, vol. 91, 2019, pp. 111–111.
Chatterjee S, Rose SJ, Mushtaq T, Cottrell E, Maharaj AV, Williams J, Savage MO, Metherell LA, Storr HL. GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon (6Ψ) mutation. HORMONE RESEARCH IN PAEDIATRICS. 2019. p. 111–111.
Journal cover image

Published In

HORMONE RESEARCH IN PAEDIATRICS

EISSN

1663-2826

ISSN

1663-2818

Publication Date

2019

Volume

91

Start / End Page

111 / 111

Related Subject Headings

  • Endocrinology & Metabolism
  • 3215 Reproductive medicine
  • 3213 Paediatrics
  • 3202 Clinical sciences
  • 1114 Paediatrics and Reproductive Medicine
  • 1103 Clinical Sciences