Cloned mice raise possibility of human cloning.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 11, doi. 10.1034/j.1399-0004.1999.550102-1.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1999 AND VI 55 AND IP 1
Results: 17
1
2
TGFA: exon–intron structure and evaluation as a candidate gene for Alström syndrome.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 61, doi. 10.1034/j.1399-0004.1999.550111.x
- By:
- Publication type:
- Article
3
Molecular therapy for genetic muscle diseases – status 1999.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 1, doi. 10.1034/j.1399-0004.1999.550101.x
- By:
- Publication type:
- Article
4
A second gene for myotonic dystrophy.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 12, doi. 10.1034/j.1399-0004.1999.550102-2.x
- By:
- Publication type:
- Article
5
Kenny–Caffey syndrome: an Arab variant?
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 44, doi. 10.1034/j.1399-0004.1999.550108.x
- By:
- Publication type:
- Article
6
To be or not to be an aggregate.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 9, doi. 10.1034/j.1399-0004.1999.550102.x
- By:
- Publication type:
- Article
7
Diversity in expression of glucose-6-phosphate dehydrogenase deficiency in females.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 13, doi. 10.1034/j.1399-0004.1999.550103.x
- By:
- Publication type:
- Article
8
Thalassemia carrier screening and prenatal diagnosis among the British Columbia (Canada) population of Chinese descent.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 20, doi. 10.1034/j.1399-0004.1999.550104.x
- By:
- Publication type:
- Article
9
How do carriers of hemophilia and their spouses experience prenatal diagnosis by chorionic villus sampling?
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 26, doi. 10.1111/j.1399-0004.1999.tb00001.x
- By:
- Publication type:
- Article
10
Nevoid basal cell carcinoma syndrome. Clinical findings in 37 Italian affected individuals.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 34, doi. 10.1034/j.1399-0004.1999.550106.x
- By:
- Publication type:
- Article
11
Lower extremity counterpart of the Poland syndrome.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 41, doi. 10.1034/j.1399-0004.1999.550107.x
- By:
- Publication type:
- Article
12
Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate-deficient glycoprotein syndrome type 1.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 50, doi. 10.1034/j.1399-0004.1999.550109.x
- By:
- Publication type:
- Article
13
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 55, doi. 10.1034/j.1399-0004.1999.550110.x
- By:
- Publication type:
- Article
14
Analysis of infertile brothers with congenital bilateral absence of vas deferens for mutations in the CFTR gene.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 63, doi. 10.1034/j.1399-0004.1999.550112.x
- By:
- Publication type:
- Article
15
Mutation in the factor V gene associated with inferior vena cava thrombosis in newborns.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 65, doi. 10.1034/j.1399-0004.1999.550113.x
- By:
- Publication type:
- Article
16
Genetic investigation of patients with hypercholesterolemia type IIa.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 67, doi. 10.1034/j.1399-0004.1999.550114.x
- By:
- Publication type:
- Article
17
Impact of ApoE4 allele on total cholesterol levels of children in northern Spain.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 1, p. 69, doi. 10.1034/j.1399-0004.1999.550115.x
- By:
- Publication type:
- Article