(Q41469765)

English

Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint

scientific article published on May 1994

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

author name string

M Chery

1

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

V Biancalana

2

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

C Philippe

3

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

G Malpuech

4

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

H Carla

5

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

S Gilgenkrantz

6

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

J L Mandel

7

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

A Hanauer

8

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 May 1994

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

93

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

587-591

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

https://scigraph.springernature.com/pub.10.1007/bf00202829

0 references

Tetany due to hypomagnesaemia with secondary hypocalcaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hypomagnesemia. Clinical, diagnostic and therapeutic studies in three children (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hypomagnesaemia, an autosomal recessive inherited disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-autosome translocations: cytogenetic characteristics and their consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parathyroid hormone secretion and responsiveness to parathyroid hormone in primary hypomagnesemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital Primary Hypomagnesemia, an Inborn Error of Metabolism?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes syndrome in a girl with X-autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the committee on the genetic constitution of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion and amplification of the HGPRT locus in Chinese hamster cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Magnesium deficiency in children]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00202829

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

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=Q41469765&oldid=1922032770"