Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient. Read more about Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient.
Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families. Read more about Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.
Familial influence on age of onset among siblings with Huntington disease. Read more about Familial influence on age of onset among siblings with Huntington disease.
Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure. Read more about Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure.
Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency. Read more about Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency.
Family pictures: growing up with a brother with X-linked severe combined immunodeficiency. Read more about Family pictures: growing up with a brother with X-linked severe combined immunodeficiency.
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. Read more about Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
Severe congenital anomalies requiring transplantation in children with Kabuki syndrome. Read more about Severe congenital anomalies requiring transplantation in children with Kabuki syndrome.
Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood. Read more about Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood.
Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia. Read more about Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia.
