A case of 46,XX dysgenesis and marked tall stature; the need for caution in interpreting array comparative genomic hybridization (CGH)

Vidya Kanamkote Narayanan, Mira Kharbanda, Malcolm Donaldson

Open source

DOI: 10.1515/jpem-2016-0182
Published: 2016-01-01
Container: Journal of Pediatric Endocrinology and Metabolism
Publisher: Walter de Gruyter GmbH
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1515/jpem-2016-0182,
  title = {A case of 46,XX dysgenesis and marked tall stature; the need for caution in interpreting array comparative genomic hybridization (CGH)},
  author = {Vidya Kanamkote Narayanan and Mira Kharbanda and Malcolm Donaldson},
  year = {2016},
  journal = {Journal of Pediatric Endocrinology and Metabolism},
  doi = {10.1515/jpem-2016-0182},
  url = {https://doi.org/10.1515/jpem-2016-0182}
}

RIS

TY  - JOUR
TI  - A case of 46,XX dysgenesis and marked tall stature; the need for caution in interpreting array comparative genomic hybridization (CGH)
AU  - Vidya Kanamkote Narayanan
AU  - Mira Kharbanda
AU  - Malcolm Donaldson
PY  - 2016
JO  - Journal of Pediatric Endocrinology and Metabolism
DO  - 10.1515/jpem-2016-0182
UR  - https://doi.org/10.1515/jpem-2016-0182
ER  -

APA

Narayanan, V. K., Kharbanda, M., & Donaldson, M. (2016). A case of 46,XX dysgenesis and marked tall stature; the need for caution in interpreting array comparative genomic hybridization (CGH). Journal of Pediatric Endocrinology and Metabolism. https://doi.org/10.1515/jpem-2016-0182

Source records

crossref · retrieved 2026-09-25T17:15:48.094Z