Literature DB >> 4141633

X-linked congenital panhypopituitarism.

R N Schimke, J J Spaulding, J G Hollowell.   

Abstract

Two half brothers with panhypopituitary dwarfism are reported who have the same mother and different, unrelated fathers. The subject of hereditary panhypopituitarism is reviewed briefly. It is concluded that there are at least two forms of hereditary panhypopituitary dwarfism, one of which may be X-linked.

Entities:  

Mesh：

Year:  1971        PMID： 4141633

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


  3 in total

1.  The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes.

Authors:  P J Douville; S Atanasoski; A Tobler; A Fontana; M E Schwab
Journal:  Mamm Genome       Date:  1994-03       Impact factor: 2.957

2.  Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3.

Authors:  N M Solomon; S A Ross; T Morgan; J L Belsky; F A Hol; P S Karnes; N J Hopwood; S E Myers; A S Tan; G L Warne; S M Forrest; P Q Thomas
Journal:  J Med Genet       Date:  2004-09       Impact factor: 6.318

3.  Recessively inherited growth hormone deficiency in a family from Iraq.

Authors:  M D Donaldson; S M Tucker; D B Grant
Journal:  J Med Genet       Date:  1980-08       Impact factor: 6.318
  3 in total

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