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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1980 | 1 |
1988 | 1 |
1992 | 1 |
1997 | 1 |
1998 | 2 |
2002 | 1 |
2024 | 0 |
PubMed (cited) for id: 244460
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Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.
Nat Genet. 2002 Nov;32(3):448-52. doi: 10.1038/ng1012. Epub 2002 Oct 21.
Nat Genet. 2002.
PMID: 12389028
The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
Diaz GA, Khan KT, Gelb BD.
Diaz GA, et al.
Genomics. 1998 Nov 15;54(1):13-8. doi: 10.1006/geno.1998.5530.
Genomics. 1998.
PMID: 9806825
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Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.
Sabry MA, Zaki M, Abul Hassan SJ, Ramadan DG, Abdel Rasool MA, al Awadi SA, al Saleh Q.
Sabry MA, et al.
J Med Genet. 1998 Jan;35(1):31-6. doi: 10.1136/jmg.35.1.31.
J Med Genet. 1998.
PMID: 9475091
Free PMC article.
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Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.
Tahseen K, Khan S, Uma R, Usha R, Al Ghanem MM, Al Awadi SA, Farag TI.
Tahseen K, et al.
Am J Med Genet. 1997 Mar 17;69(2):126-32.
Am J Med Genet. 1997.
PMID: 9056548
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[Diaphysary tubular stenosis (Kenny-Caffey's syndrome): presentation of four observations (author's transl)].
Sarría A, Toledo F, Toledo J, Vega ML, López S, Bueno M.
Sarría A, et al.
An Esp Pediatr. 1980 May;13(5):373-80.
An Esp Pediatr. 1980.
PMID: 7406361
Spanish.
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Kenny syndrome: description of additional abnormalities and molecular studies.
Bergada I, Schiffrin A, Abu Srair H, Kaplan P, Dornan J, Goltzman D, Hendy GN.
Bergada I, et al.
Hum Genet. 1988 Sep;80(1):39-42. doi: 10.1007/BF00451452.
Hum Genet. 1988.
PMID: 2843457
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Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.
Franceschini P, et al.
Am J Med Genet. 1992 Jan 1;42(1):112-6. doi: 10.1002/ajmg.1320420123.
Am J Med Genet. 1992.
PMID: 1308349
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