- PMID 27287744. S2CID 28321025. Thomson, MS. (Mar 1936). "Poikiloderma
Congenitale: Two
Cases for Diagnosis". Proc R Soc Med. 29 (5): 453–5. PMC 2076117...
- Gessain [fr]
interested himself in what he
called the
tache pigmentaire congénitale or
coloured birthmark,
publishing multiple papers in the
Journal de la...
- [page needed] Sulzberger,
Marion B (1928). "Über eine
bisher nicht beschriebene congenitale Pigmentanomalie" [About a
previously udescribed congenital pigment anomaly]...
- Lezrek,
Mounir (2014-09-30). "Pseudo-hypopion
inverse avec
polycorie congénitale". The Pan
African Medical Journal. 19: 108. doi:10.11604/pamj.2014.19...
-
Antoine Marfan (Spanish) Marfan,
Antoine (1896). "Un cas de déformation
congénitale des
quartre membres, plus prononcée aux extrémitiés, caractérisée par...
-
genomic instability. Rothmund-Thomson syndrome, also
known as
poikiloderma congenitale, is
characterized by
premature aging, skin and
skeletal abnormalities...
- synd/1662 at Who
Named It? Léri A,
Weill JA (1929). "Une
affection congénitale et symétrique du développement osseux. La dyschondrostéose". Bulletins...
- 3000 to 5000
individuals Marfan,
Antoine (1896). "Un cas de déformation
congénitale des
quartre membres, plus prononcée aux extrémitiés, caractérisée par...
-
complementation group 11)
Rombo syndrome Rothmund–Thomson
syndrome (poikiloderma
congenitale) Rud
syndrome Say
syndrome Scalp–ear–nipple
syndrome (Finlay–Marks syndrome)...
-
located on the long arm of
chromosome 8(8q22.1). Leri A (1921) Une
maladie congenitale et
hereditaire de l'ossification: la
pleonosteose familiale. Bull Mem...
