Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC).
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 97, doi. 10.1111/j.1399-0004.1991.tb02994.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1991 AND VI 39 AND IP 2
Results: 15
1
2
Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy report.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 142, doi. 10.1111/j.1399-0004.1991.tb03001.x
- By:
- Publication type:
- Article
3
Short arm deletion of chromosome 1: del(1)(p13.3 p22.3) in a female infant with an extreme tetralogy of Fallot.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 132, doi. 10.1111/j.1399-0004.1991.tb02999.x
- By:
- Publication type:
- Article
4
XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 156, doi. 10.1111/j.1399-0004.1991.tb03004.x
- By:
- Publication type:
- Article
5
Unstable translocations: a new case?
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 149, doi. 10.1111/j.1399-0004.1991.tb03002.x
- By:
- Publication type:
- Article
6
The prevalence of chromosome diseases in the general population of Sichuan, China.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 81, doi. 10.1111/j.1399-0004.1991.tb02991.x
- By:
- Publication type:
- Article
7
Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridization.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 93, doi. 10.1111/j.1399-0004.1991.tb02993.x
- By:
- Publication type:
- Article
8
Ring chromosome 4 in a child with mild dysmorphic signs.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 151, doi. 10.1111/j.1399-0004.1991.tb03003.x
- By:
- Publication type:
- Article
9
The cerebro-reno-digital syndromes: a new community.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 104, doi. 10.1111/j.1399-0004.1991.tb02995.x
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- Publication type:
- Article
10
Annual Meeting of the European Society of Human Genetics.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 159, doi. 10.1111/j.1399-0004.1991.tb03005.x
- Publication type:
- Article
11
Using the polymerase chain reaction to maintain DNA probe inventories in clinical and diagnostic laboratories.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 121, doi. 10.1111/j.1399-0004.1991.tb02997.x
- By:
- Publication type:
- Article
12
Frequency of the phenylalanine deletion (ΔF.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 89, doi. 10.1111/j.1399-0004.1991.tb02992.x
- By:
- Publication type:
- Article
13
Rapp-Hodgkin hypohidrotic ectodermal dysplasia syndrome.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 114, doi. 10.1111/j.1399-0004.1991.tb02996.x
- By:
- Publication type:
- Article
14
Counselling under genetic heterogeneity: a practical approach.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 125, doi. 10.1111/j.1399-0004.1991.tb02998.x
- By:
- Publication type:
- Article
15
Brief clinical report: a 46,XY phenotypic female with Smith-Lemli-Opitz syndrome.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 2, p. 136, doi. 10.1111/j.1399-0004.1991.tb03000.x
- By:
- Publication type:
- Article