Literature DB >> 6772660

HLA-compatible paternity in two "fertile eunuchs" with congenital hypogonadotropic hypogonadism and anosmia (the Kallmann syndrome).

A D Rogol, K K Mittal, B J White, M H McGinniss, J M Lieblich, S W Rosen.   

Abstract

Two men are described who fulfill the criteria for both the Kallmann and the fertile eunuch syndrome, and we report the erythrocyte and HLA phenotypes of these men and their children. There were no paternal exclusions noted in red blood cell phenotypes encompassing seven separate red cell systems. The HLA phenotypes indicate that the probability that these men were the fathers of the children was greater than 99.99%.

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Year:  1980        PMID: 6772660     DOI: 10.1210/jcem-51-2-275

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


  2 in total

1.  Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations.

Authors:  Eeva-Maria Laitinen; Johanna Tommiska; Timo Sane; Kirsi Vaaralahti; Jorma Toppari; Taneli Raivio
Journal:  PLoS One       Date:  2012-06-19       Impact factor: 3.240

2.  Semen quality in patients with pituitary disease and adult-onset hypogonadotropic hypogonadism.

Authors:  Mikkel Andreassen; Anders Juul; Ulla Feldt-Rasmussen; Niels Jørgensen
Journal:  Endocr Connect       Date:  2018-03-07       Impact factor: 3.335

  2 in total

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