(Q35626152)

9 August 2017

title

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features (English)

1 reference

9 August 2017

0 references

1 reference

Sanjad SA

1

1 reference

9 August 2017

Sakati NA

2

1 reference

9 August 2017

Abu-Osba YK

3

1 reference

9 August 2017

Kaddoura R

4

1 reference

9 August 2017

Milner RD

5

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 February 1991

1 reference

Archives of Disease in Childhood

9 August 2017

published in

1 reference

9 August 2017

volume

66

1 reference

9 August 2017

issue

2

1 reference

9 August 2017

page(s)

193-196

1 reference

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Partial monosomy of chromosome 10 short arms.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Exclusion of close linkage between the parathyroid hormone gene and a mutant gene locus causing idiopathic hypoparathyroidism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Familial isolated hypoparathyroidism: a molecular genetic analysis of 8 families with 23 affected persons.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Short stature, mental retardation, and hypoparathyroidism: a new syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Familial nephrosis, nerve deafness, and hypoparathyroidism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

The spectrum of the DiGeorge syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792808

Partial monosomy 10p syndrome

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2001103

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Silver-Russell syndrome with unusual findings

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2001103

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

HEREDITARY HYPOPARATHYROIDISM PRESENTING WITH OEDEMA IN THE NEONATAL PERIOD

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2001103

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.66.2.193

1 reference

9 August 2017

1 reference

9 August 2017

1 reference