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5. An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis. Maya-Nuñez G; Torres L; Ulloa-Aguirre A; Zenteno JC; Cuevas-Covarrubias S; Saavedra-Ontiveros D; Kofman-Alfaro S; Méndez JP Clin Endocrinol (Oxf); 1999 Feb; 50(2):157-62. PubMed ID: 10396356 [TBL] [Abstract][Full Text] [Related]
6. Identification of olfactory dysfunction in carriers of X-linked Kallmann's syndrome. Kirk JM; Grant DB; Savage MO; Besser GM; Bouloux PM Clin Endocrinol (Oxf); 1994 Nov; 41(5):577-80. PubMed ID: 7828345 [TBL] [Abstract][Full Text] [Related]
7. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus. Bouloux PM; Kirk J; Munroe P; Duke V; Meindl A; Hilson A; Grant D; Carter N; Betts D; Meitinger T Clin Genet; 1993 Apr; 43(4):169-73. PubMed ID: 8330450 [TBL] [Abstract][Full Text] [Related]
8. X-linked Kallmann syndrome and renal agenesis occurring together and independently in a large Australian family. Colquhoun-Kerr JS; Gu WX; Jameson JL; Withers S; Bode HH Am J Med Genet; 1999 Mar; 83(1):23-7. PubMed ID: 10076881 [TBL] [Abstract][Full Text] [Related]
9. Proteinuria, hypertension and chronic renal failure in X-linked Kallmann's syndrome, a defined genetic cause of solitary functioning kidney. Duke V; Quinton R; Gordon I; Bouloux PM; Woolf AS Nephrol Dial Transplant; 1998 Aug; 13(8):1998-2003. PubMed ID: 9719154 [TBL] [Abstract][Full Text] [Related]
11. A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome. Maya-Nuñez G; Zenteno JC; Ulloa-Aguirre A; Kofman-Alfaro S; Mendez JP J Clin Endocrinol Metab; 1998 May; 83(5):1650-3. PubMed ID: 9589672 [TBL] [Abstract][Full Text] [Related]
12. Renal abnormalities in patients with Kallmann syndrome. Zenteno JC; Méndez JP; Maya-Núñez G; Ulloa-Aguirre A; Kofman-Alfaro S BJU Int; 1999 Mar; 83(4):383-6. PubMed ID: 10210557 [TBL] [Abstract][Full Text] [Related]
13. Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome. Ballabio A; Sebastio G; Carrozzo R; Parenti G; Piccirillo A; Persico MG; Andria G Hum Genet; 1987 Dec; 77(4):338-41. PubMed ID: 3480263 [TBL] [Abstract][Full Text] [Related]
14. Novel homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family. Xu H; Li Z; Wang T; Wang S; Liu J; Wang DW Andrologia; 2015 Dec; 47(10):1160-5. PubMed ID: 25597551 [TBL] [Abstract][Full Text] [Related]
15. Kallmann's syndrome with unilateral renal agenesis. A case report. Honiball S; Sandler M S Afr Med J; 1986 Oct; 70(8):489-91. PubMed ID: 2877504 [TBL] [Abstract][Full Text] [Related]
16. KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development. Duke VM; Winyard PJ; Thorogood P; Soothill P; Bouloux PM; Woolf AS Mol Cell Endocrinol; 1995 Apr; 110(1-2):73-9. PubMed ID: 7545624 [TBL] [Abstract][Full Text] [Related]
17. [X-linked Kallmann's syndrome: intra and interfamilial heterogeneity]. Vidal A; Loidi L; Colino E; del Carmen Miranda M; Barrio R Med Clin (Barc); 2007 May; 128(20):777-9. PubMed ID: 17568506 [TBL] [Abstract][Full Text] [Related]
18. Renal agenesis in Kallmann syndrome: a network approach. Tickotsky N; Moskovitz M Ann Hum Genet; 2014 Nov; 78(6):424-33. PubMed ID: 25227403 [TBL] [Abstract][Full Text] [Related]
19. The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis. Quinton R; Duke VM; de Zoysa PA; Platts AD; Valentine A; Kendall B; Pickman S; Kirk JM; Besser GM; Jacobs HS; Bouloux PM J Clin Endocrinol Metab; 1996 Aug; 81(8):3010-7. PubMed ID: 8768867 [TBL] [Abstract][Full Text] [Related]