Familial occurrence of supravalvular aortic stenosis.
Explore the source record for details and available documents.
Adolescent↗
Biomedical subjects
C Zavala
Publications and source records attributed to C Zavala.
[Chromosome changes in mental patients. Study in 2 psychiatric hospitals].
Explore the source record for details and available documents.
Adolescent↗
[Type E brachydactylia and harelip in the same family].
Explore the source record for details and available documents.
Adult↗
[Tables to calculate the probability of mono dizygoticity in twins. Study of Mexican population groups].
Explore the source record for details and available documents.
Female↗
[Sex chromosome aberrations in imprisoned women. Study in the Women's Prison of Mexico City].
Explore the source record for details and available documents.
Adolescent↗
[Chronic hereditary nephropathy with hypoacusia and ocular defects (study of a family)].
Explore the source record for details and available documents.
Adolescent↗
[Chromosome studies in a Mexican prison].
Explore the source record for details and available documents.
Body Height↗
[Chromosome studies in a Mexican prison].
Explore the source record for details and available documents.
Crime↗
Absence of the XYY syndrome amongst 164 police force students in Mexico City.
Explore the source record for details and available documents.
Adolescent↗
Syndactyly type I in six generations of a large Mexican family.
Explore the source record for details and available documents.
Female↗
Estimation of the number of females at risk of isoimmunization to the Rho (D) antigen in a sample of the population attended at the Instituto Mexicano del Seguro Social.
Explore the source record for details and available documents.
ABO Blood-Group System↗
Clinical use of "somatometric profiles" and the effect of polygenic inheritance for stature in patients with bone dysplasias.
Explore the source record for details and available documents.
Adolescent↗
Differences in recurrence risk for siblings for cleft lip and/or palate depending on the degree of the malformation and on family history.
Explore the source record for details and available documents.
Adolescent↗
[Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
The severe Duchenne type of muscular dystrophy is inherited as an X-linked recessive trait. Approximately two thirds of healthy female heterozygous carriers have a high serum creatine kinase (SCK). A suspected carrier with a normal SCK level therefore, presents an important problem in genetic counselling. Based on Bayesian methods, Emery and Hollyway derived a formula which is applicable when the sporadic case is either the son or brother of a consultant and which also includes information on SCK levels in the consultant and in normal daughters and sisters. The present paper describes the results obtained with use of this formula in 27 families with at least a propositus with Duchenne muscular dystrophy.
Adolescent↗
[The biological concept of race].
Explore the source record for details and available documents.
Blood Group Antigens↗
[Genetic analysis of 127 families with vitiligo (author's transl)].
Explore the source record for details and available documents.
Female↗