Endocrine and exocrine pancreatic function and the ΔF508 mutation in cystic fibrosis.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 345, doi. 10.1111/j.1399-0004.1991.tb03107.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1991 AND VI 40 AND IP 5
Results: 7
1
2
Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental field.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 349, doi. 10.1111/j.1399-0004.1991.tb03108.x
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- Publication type:
- Article
3
X-linked mental retardation with bilateral clasped thumbs: report of another affected family.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 337, doi. 10.1111/j.1399-0004.1991.tb03105.x
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- Publication type:
- Article
4
23rd Annual Symposium of the European Society of Human Genetics July 13-16, 1991 Leuven, Belgium.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 359, doi. 10.1111/j.1399-0004.1991.tb03111.x
- Publication type:
- Article
5
Announcements.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 358, doi. 10.1111/j.1399-0004.1991.tb03110.x
- Publication type:
- Article
6
Nasopalpebral lipoma-coloboma syndrome.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 342, doi. 10.1111/j.1399-0004.1991.tb03106.x
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- Publication type:
- Article
7
Mosaic tetraploidy in a liveborn infant with features of the DiGeorge anomaly.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 5, p. 353, doi. 10.1111/j.1399-0004.1991.tb03109.x
- By:
- Publication type:
- Article