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49, XXXXY syndrome in a 1 year-old infant.

Abstract

Clinical signs of developmental anomalies found in the 49, XXXXY patients have been reported based on the author's case.

Authors

, ,

Source

Klinische Padiatrie 189:6 1977 Nov pg 477-81

MeSH

Abnormalities, Multiple
Bone Diseases, Developmental
Female
Humans
Hypogonadism
Infant
Intellectual Disability
Karyotyping
Male
Sex Chromosome Aberrations
X Chromosome

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

563945

Citation

Molska, I, et al. "49, XXXXY Syndrome in a 1 Year-old Infant." Klinische Padiatrie, vol. 189, no. 6, 1977, pp. 477-81.
Molska I, Lech H, Wiśniewski L. 49, XXXXY syndrome in a 1 year-old infant. Klin Padiatr. 1977;189(6):477-81.
Molska, I., Lech, H., & Wiśniewski, L. (1977). 49, XXXXY syndrome in a 1 year-old infant. Klinische Padiatrie, 189(6), pp. 477-81.
Molska I, Lech H, Wiśniewski L. 49, XXXXY Syndrome in a 1 Year-old Infant. Klin Padiatr. 1977;189(6):477-81. PubMed PMID: 563945.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - 49, XXXXY syndrome in a 1 year-old infant. AU - Molska,I, AU - Lech,H, AU - Wiśniewski,L, PY - 1977/11/1/pubmed PY - 1977/11/1/medline PY - 1977/11/1/entrez SP - 477 EP - 81 JF - Klinische Padiatrie JO - Klin Padiatr VL - 189 IS - 6 N2 - Clinical signs of developmental anomalies found in the 49, XXXXY patients have been reported based on the author's case. SN - 0300-8630 UR - https://www.unboundmedicine.com/medline/citation/563945/49_XXXXY_syndrome_in_a_1_year_old_infant_ DB - PRIME DP - Unbound Medicine ER -