Hirschsprung's disease, distinctive facies, and microcephaly.
- 1 April 1989
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 26 (4) , 287-288
- https://doi.org/10.1136/jmg.26.4.287
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration.Journal of Medical Genetics, 1988
- Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.Journal of Medical Genetics, 1988
- Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).Journal of Medical Genetics, 1988
- Smith‐Lemli‐Opitz syndrome‐type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethalityAmerican Journal of Medical Genetics, 1987
- Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generations.1983
- Hirschsprung megacolon and cleft palate in two sibs.1981
- Hirschsprung's disease and Waardenburg's syndrome.1979
- Hirschsprung's Disease and Waardenburg's SyndromePublished by American Academy of Pediatrics (AAP) ,1979
- Hirschsprung's disease and congenital deafnessHuman Genetics, 1977
- Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy.Journal of Medical Genetics, 1975