(Q41678345)

7 October 2017

Hirschsprung's disease, distinctive facies, and microcephaly (English)

1 reference

7 October 2017

0 references

Hirschsprung's disease

1 reference

Bankier A

1

1 reference

PMCID

1017307

7 October 2017

language of work or name

English

0 references

publication date

1 April 1989

1 reference

Journal of Medical Genetics

7 October 2017

1 reference

7 October 2017

26

1 reference

7 October 2017

4

1 reference

7 October 2017

287-288

1 reference

Hirschsprung megacolon and cleft palate in two sibs

7 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generations.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22)

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Hirschsprung's disease and Waardenburg's syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017307

Hirschsprung's disease and congenital deafness. Familial assocation

6 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2716039

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

0 references

1 reference

7 October 2017

1 reference

PMCID

1017307