TY  - GEN
AU  - Bonneau,D
AU  - Huret,J L
AU  - Godeau,G
AU  - Couet,D
AU  - Putterman,M
AU  - Tanzer,J
AU  - Babin,P
AU  - Larrègue,M
TI  - Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype
SN  - 0340-6717
PY  - 1991///0912
KW  - Cells, Cultured
KW  - Chromosomes, Human, Pair 7
KW  - Cutis Laxa
KW  - genetics
KW  - Female
KW  - Humans
KW  - Immunoenzyme Techniques
KW  - Infant
KW  - Karyotyping
KW  - Laminin
KW  - Marfan Syndrome
KW  - Phenotype
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1007/BF00200911
ER  -