Editorial: Turner's and Noonan's syndromes.
出版信息
Br Med J. 1974 Mar 16;1(5906):470-1. doi: 10.1136/bmj.1.5906.470-a.
Abstract
摘要
相似文献
1
Editorial: Turner's and Noonan's syndromes.
Br Med J. 1974 Mar 16;1(5906):470-1. doi: 10.1136/bmj.1.5906.470-a.
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Cardiovascular malformations in Turner's and Noonan's syndrome.
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[Somatometric profile of female patients with Turner's syndrome and male and female patients with Noonan's syndrome].
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[3 recent cases of Noonan's syndrome].
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Turner syndrome and Noonan's syndrome.
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[Turner's phenotype and diagnosis of Noonan's syndrome].
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Noonan's syndrome associated with polycistic renal disease.
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[Turner's phenotype syndrome (Noonan's syndrome)].
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[Rare morphological anomalies of the urinary tract in Turner's syndrome].
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本文引用的文献
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KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.
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THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS.
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Multiple congenital defects in a twelve year old boy with cryptorchidism--"male Turner's syndrome".
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A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).
Lancet. 1959 Apr 4;1(7075):711-3. doi: 10.1016/s0140-6736(59)91893-8.
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Ullrich-Turner syndrome in the male: review of the literature and report of a case with lymphocytic (Hashimoto's) thyroiditis.
Mayo Clin Proc. 1966 Dec;41(12):843-54.
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Turner syndrome and Noonan's syndrome.
J Pediatr. 1969 Jan;74(1):155-6. doi: 10.1016/s0022-3476(69)80027-2.
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Congenital heart disease in male and female subjects with somatic features of Turner's syndrome and normal sex chromosomes (Ullrich's and related syndromes).
Br Heart J. 1972 Jan;34(1):41-6. doi: 10.1136/hrt.34.1.41.
8
Pulmonary stenosis in patients with the Turner phenotype in the male.
Am J Dis Child. 1968 Oct;116(4):351-8. doi: 10.1001/archpedi.1968.02100020355002.
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The appearance of the left ventricle in Noonan's syndrome.
Radiology. 1973 Oct;109(1):155-9. doi: 10.1148/109.1.155.
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Cardiomyopathy in Noonan's syndrome. Report of 3 cases.
Br Heart J. 1973 Jan;35(1):99-102. doi: 10.1136/hrt.35.1.99.
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