1.
J. bras. med
;
46(1): 13-29, 1984.
Article
in Portuguese
| LILACS
| ID: lil-20617
Subject(s)
Pregnancy , Infant, Newborn , Humans , Male , Female , Chromosome Aberrations , Down Syndrome , Genetic Counseling , Prenatal Diagnosis
2.
J. pediatr. (Rio J.)
;
56(1/2): 25-9, 1984.
Article
in Portuguese
| LILACS
| ID: lil-21832
Subject(s)
Infant , Humans , Male , Abnormalities, Multiple , Cytogenetics , Infant, Low Birth Weight , Microcephaly , Intellectual Disability
3.
Rev. bras. neurol
;
19(4): 93-6, 1984.
Article
in Portuguese
| LILACS
| ID: lil-24152
ABSTRACT
Os AA. estudam uma familia com a doenca de Charcot-Marie-Tooth, na qual se verifica forma rara de transmissao genetica: dominante ligada ao cromossoma X. A concomitancia com a anemia falciforme e comentada. O aconselhamento genetico, motivo que levou o proposito a consulta, e analisado em seus diferentes aspectos
Subject(s)
Child, Preschool , Child , Adolescent , Adult , Humans , Male , Female , Anemia, Sickle Cell , Charcot-Marie-Tooth Disease , Sex Chromosome Aberrations , X Chromosome
4.
J. pediatr. (Rio J.)
;
51(2): 124-6, 1981.
Article
in Portuguese
| LILACS
| ID: lil-6410