Header Logo

Connection

Hafiz Muhammad Jafar Hussain to Kallmann Syndrome

Back to Details
This is a "connection" page, showing publications Hafiz Muhammad Jafar Hussain has written about Kallmann Syndrome.
Hafiz Muhammad Jafar Hussain
Connection Strength
0.640
Kallmann Syndrome
  1. Whole Exome Sequencing Revealed a Novel Nonsense Variant in the GNRHR Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family. Horm Res Paediatr. 2019; 91(1):9-16.
    View in: PubMed
    Score: 0.640
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.