SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

ALAGILLE SYNDROME - FAMILY STUDIES

Elmslie, FV; Vivian, AJ; Gardiner, H; Hall, C; Mowat, AP; Winter, RM (1995) ALAGILLE SYNDROME - FAMILY STUDIES. JOURNAL OF MEDICAL GENETICS, 32 (4). 264 - 268 (5). ISSN 0022-2593 https://doi.org/10.1136/jmg.32.4.264
SGUL Authors: Elmslie, Frances

Full text not available from this repository.
Item Type: Article
Additional Information: PubMed ID: 7643353
Keywords: Abortion, Spontaneous, Alagille Syndrome, Child, Family Health, Fathers, Female, Genes, Dominant, Heterozygote, Humans, Male, Mothers, Pedigree, Pregnancy, Severity of Illness Index, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, ARTERIOHEPATIC DYSPLASIA, MALFORMATIONS, DELETION, 20P
Journal or Publication Title: JOURNAL OF MEDICAL GENETICS
ISSN: 0022-2593
Related URLs:
Dates:
DateEvent
1 April 1995Published
Web of Science ID: WOS:A1995QU52800004
Download EPMC Full text (PDF)
Download EPMC Full text (HTML)
URI: https://openaccess.sgul.ac.uk/id/eprint/148
Publisher's version: https://doi.org/10.1136/jmg.32.4.264

Actions (login required)

Edit Item Edit Item