Literature DB >> 4982597

A TBG-deficient family with a male exhibiting decreased but not zero TBG levels.

R C Roberts, T F Nikolai, F N Lohrenz.   

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Year:  1970        PMID： 4982597     DOI： 10.1210/jcem-30-1-131

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  6 in total

1.  Thyroid-binding globulin deficiency in a patient with Beckwith's syndrome.

Authors:  S L Kaufman; R Frederickson
Journal:  Calif Med       Date:  1973-04

2.  X-chromosome linked inheritance of decreased thyroxine-binding globulin.

Authors:  P Malvaux; P De Nayer
Journal:  Arch Dis Child       Date:  1972-08       Impact factor: 3.791

3.  Growth retardation and thyroxine-binding globulin deficiency.

Authors:  J L Penfold; G M Kneebone; M Wellby; R K Oldfield
Journal:  Arch Dis Child       Date:  1971-02       Impact factor: 3.791

4.  Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female.

Authors:  M Bigazzi; R Ronga; A L Olivotti; G Scarselli; S Refetoff
Journal:  J Endocrinol Invest       Date:  1980 Oct-Dec       Impact factor: 4.256

5.  Study of four new kindreds with inherited thyroxine-binding globulin abnormalities. Possible mutations of a single gene locus.

Authors:  S Refetoff; N I Robin; C A Alper
Journal:  J Clin Invest       Date:  1972-04       Impact factor: 14.808

6.  The genetic polymorphism of the thyroxine-binding globulin (TBG).

Authors:  J Köbberling; D Emrich
Journal:  Humangenetik       Date:  1972
  6 in total

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