Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype.

Bonneau, D

Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype. [electronic resource] - Human genetics Jul 1991 - 317-9 p. digital

Publication Type: Case Reports; Journal Article

0340-6717

10.1007/BF00200911 doi


Cells, Cultured
Chromosomes, Human, Pair 7
Cutis Laxa--genetics
Female
Humans
Immunoenzyme Techniques
Infant
Karyotyping
Laminin--genetics
Marfan Syndrome--genetics
Phenotype