The DOI matches its Crossref record; 114 of the 114 references it cites were found in a registry or an index.
Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features
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Citations
Cites
Sinclair, A. H., Berta, P., Palmer, M. S., Hawkins, J. R., Griffiths, B. L., Smith, M. J., Foster, J. W., Frischauf, A.-M., Lovell-Badge, R., & Goodfellow, P. N. (1990) · Nature · doi:10.1038/346240a0 · Cited by 3,236
Tanner, J. M., Whitehouse, R. H., & Takaishi, M. (1966) · Archives of Disease in Childhood · doi:10.1136/adc.41.220.613 · Cited by 2,553
Human Genetics. Problems and Approaches.
(1980) · Annals of Internal Medicine · doi:10.7326/0003-4819-93-1-163_3 · Cited by 991
Prader, A., Largo, R. H., Molinari, L., & Issler, C. (1989) · PubMed · Cited by 677
Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions
Boué, J., Boué, A., & Lazar, P. (1975) · Teratology · doi:10.1002/tera.1420120103 · Cited by 661
Malaparte, C. (1988) · Cited by 601
NCHS growth curves for children birth-18 years. United States.
Hamill, P. V. V., Drizd, T. A., Johnson, C. L., Reed, R. B., & Roche, A. F. (1977) · PubMed · Cited by 582
The anatomy and histology of XO human embryos and fetuses
Singh, R. P., & Carr, D. H. (1966) · The Anatomical Record · doi:10.1002/ar.1091550309 · Cited by 450
Congenital anomalies in the newborninfant, including minor variations
Marden, P. M., Smith, D. W., & McDonald, M. J. (1964) · The Journal of Pediatrics · doi:10.1016/s0022-3476(64)80188-8 · Cited by 422
A human XY female with a frame shift mutation in the candidate testis-determining gene SRY
Jäger, R. J., Anvret, M., Hall, K., & Scherer, G. (1990) · Nature · doi:10.1038/348452a0 · Cited by 408
Cited by
Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome
Stochholm, K., Juul, S., Juel, K., Naeraa, R. W., & Højbjerg Gravholt, C. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-0558 · Cited by 652
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
Clement-Jones, M. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.5.695 · Cited by 423
Pregnancy in patients with Turner's syndrome: six new cases and review of literature
Tarani, L., Lampariello, S., Raguso, G., Colloridi, F., Pucarelli, I., Pasquino, A. M., & Bruni, L. A. (1998) · Gynecological Endocrinology · doi:10.3109/09513599809024955 · Cited by 228
Epigenetics in Turner syndrome
Álvarez-Nava, F., & Lanes, R. (2018) · Clinical Epigenetics · doi:10.1186/s13148-018-0477-0 · Cited by 79
Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children
Bilge, I., Kayserili, H., Emre, S., Nayir, A., Sirin, A., Tukel, T., Bas, F., Kilic, G., Basaran, S., Gunoz, H., et al. (2000) · Pediatric Nephrology · doi:10.1007/s004670000315 · Cited by 77
Metadata
- Authors
- Ogata, T., & Matsuo, N.
- Venue
- Human Genetics
- Published
- 1995-06
- Volume
- 95
- Issue
- 6
- Pages
- 607-29
- ISSN
- 0018-7348 (ISSN-L)
- 0340-6717
- 1432-1203
- OpenAlex
- W1987097380
- Cited by
- 277
- References
- 114
- FWCI
- 7.30
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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- CoChat. (2026). Citation check: Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. https://app.cochat.ai/papers/10.1007/bf00209476
- The paper
- Ogata, T., & Matsuo, N. (1995). Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. Human Genetics. https://doi.org/10.1007/bf00209476
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
