Kallmann syndrome in two sisters with other developmental anomalies also affecting their father
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb04451.x/fullpdf
Reference13 articles.
1. Chromosome abnormality in Kallmann syndrome;Best;Am J Med Genet,1990
2. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules;Franco;Nature,1991
3. Kallmann syndrome due to a translocation resulting in an X/Y fusion gene;Guioli;Nature Genetics,1992
4. Characteristic craniofacial appearance and brachytelephalangy in a mother and son with Kallmann syndrome in the son;Hunter;Am J Med Genet,1986
5. A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism;Johnson;Am J Med Genet,1983
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