"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

scientific article

"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/AJMG.10226.ABS
P698PubMed publication ID11891681

P50authorAnita RauchQ21253643
Gabriele Gillessen-KaesbachQ30170221
P2093author name stringBeate Albrecht
Christiane Zweier
Beate Mitulla
Hans-Dieter Rott
Maike Beese
Rolf Behrens
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectcongenital disorderQ727096
P304page(s)177-181
P577publication date2002-03-01
P1433published inAmerican Journal of Medical Genetics Part AQ15755121
P1476title"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene
P478volume108