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Fetal Genotype-Phenotype Sex Discordance: A Case of 5-Alpha-Reductase Deficiency.
Fetal Pediatr Pathol. 2022 Oct;41(5):794-799. doi: 10.1080/15513815.2021.1948645. Epub 2021 Jul 12.
Fetal Pediatr Pathol. 2022.
PMID: 34251982
Observed Frequency and Characteristics of Hearing Loss in Osteogenesis Imperfecta.
Waissbluth S, Lira K, Aracena K, Oyarzun J, Willson M, Seiltgens C.
Waissbluth S, et al. Among authors: seiltgens c.
Rev Med Chil. 2020 Dec;148(12):1781-1786. doi: 10.4067/S0034-98872020001201781.
Rev Med Chil. 2020.
PMID: 33844744
Free article.
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Craniocervical abnormalities in osteogenesis imperfecta type V.
Ludwig K, Seiltgens C, Ibba A, Saran N, Ouellet JA, Glorieux F, Rauch F.
Ludwig K, et al. Among authors: seiltgens c.
Osteoporos Int. 2022 Jan;33(1):177-183. doi: 10.1007/s00198-021-06088-x. Epub 2021 Aug 5.
Osteoporos Int. 2022.
PMID: 34350492
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Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles.
Rauch D, Robinson ME, Seiltgens C, Sutton VR, Lee B, Glorieux F, Rauch F.
Rauch D, et al. Among authors: seiltgens c.
Bone. 2020 Nov;140:115547. doi: 10.1016/j.bone.2020.115547. Epub 2020 Jul 27.
Bone. 2020.
PMID: 32730936
Free PMC article.
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[Clinical features of Chilean patients with Fibrous Dysplasia/McCune-Albright Syndrome].
Jiménez C, Schneider P, Baudrand R, García H, Martínez A, Mendoza C, Grob F, Seiltgens C, Florenzano P.
Jiménez C, et al. Among authors: seiltgens c.
Rev Med Chil. 2022 Oct;150(10):1275-1282. doi: 10.4067/S0034-98872022001001275.
Rev Med Chil. 2022.
PMID: 37358085
Free article.
Spanish.
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