Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype [3]

G. Gillessen-Kaesbach^*, B. Horsthemke

^*Korrespondierende/r Autor/-in für diese Arbeit

10 Zitate (Scopus)

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

@article{7632b69ae7e349f68a14e4031b10daf2,

title = "Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype [3]",

author = "G. Gillessen-Kaesbach and B. Horsthemke",

year = "1994",

language = "English",

volume = "31",

pages = "260--261",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "3",

}

TY - JOUR

T1 - Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype [3]

AU - Gillessen-Kaesbach, G.

AU - Horsthemke, B.

PY - 1994

Y1 - 1994

UR - https://www.scopus.com/pages/publications/0028345788

M3 - Letters

C2 - 8014984

AN - SCOPUS:0028345788

SN - 0022-2593

VL - 31

SP - 260

EP - 261

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 3

ER -