53 citations
,
May 1996 in “The Journal of Clinical Endocrinology & Metabolism” Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.
76 citations
,
January 1998 in “Mammalian Genome” 3 citations
,
June 2017 in “Reproductive biomedicine online” A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.
February 2026 in “Zenodo (CERN European Organization for Nuclear Research)” February 2026 in “Zenodo (CERN European Organization for Nuclear Research)” May 2024 in “Clinical and experimental optometry”
January 2025 in “Dermatology Reports” Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.
13 citations
,
September 2011 in “International Urology and Nephrology”
July 2004 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not available for parsing.
January 2008 in “Hair transplant forum international” The document's conclusion cannot be provided as the content is not available.
June 2019 in “Reactions Weekly”
3 citations
,
January 2018 in “Postępy Dermatologii i Alergologii” Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.
June 2023 in “Zenodo (CERN European Organization for Nuclear Research)”
September 1998 in “Hair transplant forum international” The document could not be processed for a summary.
September 2024 in “Frontiers in Genetics” A specific genetic marker is linked to male pattern baldness in Han Chinese men.
September 2013 in “Hair transplant forum international” The conclusion cannot be provided because the document is not accessible.
2 citations
,
July 1996 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not accessible or understandable.
November 2018 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not accessible.
28 citations
,
March 2010 in “British Journal of Dermatology” Genetic marker rs12558842 strongly linked to male hair loss.
January 2022 in “International journal of dermatology and venereology” A Chinese man with KID syndrome had a new mutation in the GJB2 gene.
March 2024 in “Research Square (Research Square)” The TT genotype of a specific SNP in sheep is linked to better wool quality.
January 2018 in “Journal of analytical, bioanalytical and separation techniques”
September 2023 in “Journal of The American Academy of Dermatology” Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.
August 2023 in “Zenodo (CERN European Organization for Nuclear Research)” February 2006 in “Inpharma Weekly” 7 citations
,
February 2011 in “Journal of dermatology” The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.
November 2001 in “Hair transplant forum international” The document's conclusion cannot be provided because the document is not readable.
August 2023 in “Zenodo (CERN European Organization for Nuclear Research)”
November 1995 in “Hair transplant forum international” The document cannot be understood or processed.