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
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| 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: |
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| Dates: |
| Date | Event |
|---|
| 1 April 1995 | Published |
|
| Web of Science ID: |
WOS:A1995QU52800004 |
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| URI: |
https://openaccess.sgul.ac.uk/id/eprint/148 |
| Publisher's version: |
https://doi.org/10.1136/jmg.32.4.264 |
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