On the origin of extra isochromosomes.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 540, doi. 10.1111/j.1399-0004.1986.tb00557.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1986 AND VI 29 AND IP 6
Results: 16
1
2
ERRATUM.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 544, doi. 10.1111/j.1399-0004.1986.tb00561.x
- Publication type:
- Article
3
Craniofrontonasal dysplasia: clinical and genetic analysis.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 508, doi. 10.1111/j.1399-0004.1986.tb00552.x
- By:
- Publication type:
- Article
4
DNA polymorphisms around the apo Al gene in normal and hyperlipidaemic individuals selected for a twin study.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 485, doi. 10.1111/j.1399-0004.1986.tb00548.x
- By:
- Publication type:
- Article
5
Segregation analysis of brown oculocutaneous albinism.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 496, doi. 10.1111/j.1399-0004.1986.tb00550.x
- By:
- Publication type:
- Article
6
7th International Congress of Human Genetics - Satellite Workshop.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 543, doi. 10.1111/j.1399-0004.1986.tb00559.x
- Publication type:
- Article
7
Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 491, doi. 10.1111/j.1399-0004.1986.tb00549.x
- By:
- Publication type:
- Article
8
Reciprocal effects of apolipoprotein E alleles (ε2 AND ε4) on plasma lipid levels in normolipidemic subjects.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 477, doi. 10.1111/j.1399-0004.1986.tb00547.x
- By:
- Publication type:
- Article
9
First trimester chorionic villi sampling and direct chromosome preparations.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 502, doi. 10.1111/j.1399-0004.1986.tb00551.x
- By:
- Publication type:
- Article
10
Third International Conference on Chorionic Villus Sampling and Early Prenatal Diagnosis.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 543, doi. 10.1111/j.1399-0004.1986.tb00560.x
- Publication type:
- Article
11
A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 530, doi. 10.1111/j.1399-0004.1986.tb00555.x
- By:
- Publication type:
- Article
12
Critical segment for 9p deletion syndrome.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 541, doi. 10.1111/j.1399-0004.1986.tb00558.x
- By:
- Publication type:
- Article
13
The Grant Syndrome: Persistent Wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia - an autosomal dominant trait.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 523, doi. 10.1111/j.1399-0004.1986.tb00554.x
- By:
- Publication type:
- Article
14
The Human Gene Map 15 April 1986: The Morbid Anatomy of the Human Genome.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 545, doi. 10.1111/j.1399-0004.1986.tb00562.x
- By:
- Publication type:
- Article
15
Xp21/autosome translocations.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 516, doi. 10.1111/j.1399-0004.1986.tb00553.x
- By:
- Publication type:
- Article
16
Partial deletion of the short arm of chromosome 3.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 6, p. 538, doi. 10.1111/j.1399-0004.1986.tb00556.x
- By:
- Publication type:
- Article