Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH. (Q52206897)

From Wikidata

Jump to navigation Jump to search

scientific article published in August 1995

Language	Label	Description	Also known as
English	Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.	scientific article published in August 1995

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH. (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

7

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

Michael P. Whyte

2

object named as

M P Whyte

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

author name string

D Trump

1

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

C Wooding

3

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

J T Pang

4

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

S H Pearce

5

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

D B Kocher

6

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

publication date

1 August 1995

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

96

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

2

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

183-187

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the D11S480 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human parathyroid hormone gene (PTH) is on short arm of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cloning of a family of genes that encode the melanocortin receptors

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage map of the human genome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second-generation linkage map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2).

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetranucleotide repeat polymorphism at the human prostatic acid phosphatase (ACPP) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT) n polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and mapping of a polymorphic DNA sequence pJCZ3.1 on chromosome 19 [D19S20]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial benign hypercalcemia (hypocalciuric hypercalcemia). Clinical and pathogenetic studies in 21 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and characterization of an extracellular Ca(2+)-sensing receptor from bovine parathyroid

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the D3S196 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial benign hypercalcaemia. Study of a large family

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7635467

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00207376

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/7635467

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q52206897&oldid=2254981474"