Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: Expanding the phenotype of Cumming syndrome-Reference-Cited by-同舟云学术

Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: Expanding the phenotype of Cumming syndrome

Published:1997-12-31 Issue:4 Volume:73 Page:419-424
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Ming Jeffrey E.,McDonald-McGinn Donna M.,Markowitz Richard I.,Ruchelli Eduardo,Zackai Elaine H.

Publisher

Wiley

Subject

Genetics(clinical)

Reference24 articles.

1. Polydactyly, campomelia, ambiguous genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents: A new multiple malformation syndrome, or a severe form of oral-facial-digital syndrome type IV?

2. Heterotaxia syndrome and autosomal dominant inheritance

3. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family

4. Long-Limbed Campomelic Dwarfism

5. Ellis-van creveld syndrome, Jeune syndrome, and renal-hepatic-pancreatic dysplasia: separate entities or disease spectrum?

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