Found: 8
Select item for more details and to access through your institution.
Peutz-Jeghers syndrome with feminizing sertoli cell tumor.
- Published in:
- 1980
- By:
- Publication type:
- journal article
(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French–German population.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 3, p. 357, doi. 10.1038/sj.ejhg.5200298
- By:
- Publication type:
- Article
Nine independent F9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline.
- Published in:
- Human Mutation, 2000, v. 15, n. 1, p. 116, doi. 10.1002/(SICI)1098-1004(200001)15:1<116::AID-HUMU25>3.0.CO;2-N
- By:
- Publication type:
- Article
Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombin ants.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 2, p. 97, doi. 10.1111/j.1399-0004.1987.tb02776.x
- By:
- Publication type:
- Article
Cortical blindness, growth and psychomotor retardation and postaxial Polydactyly: A probably distinct autosomal recessive syndrome.
- Published in:
- Clinical Genetics, 1985, v. 28, n. 3, p. 251, doi. 10.1111/j.1399-0004.1985.tb00395.x
- By:
- Publication type:
- Article
Monosomy 16q: a distinct syndrome Apropos of a de novo del(16) (q2100q2300).
- Published in:
- Clinical Genetics, 1985, v. 28, n. 1, p. 84, doi. 10.1111/j.1399-0004.1985.tb01223.x
- By:
- Publication type:
- Article
De novo t(4;5) (q3100; q2200) with del(5)(q1500q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segment.
- Published in:
- Clinical Genetics, 1985, v. 27, n. 1, p. 105, doi. 10.1111/j.1399-0004.1985.tb00193.x
- By:
- Publication type:
- Article
Autosomal recessive onychotrichodysplasia, chronic neutropenia and mild mental retardation.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 147, doi. 10.1111/j.1399-0004.1979.tb01753.x
- By:
- Publication type:
- Article