(Q46391702)

English

Chromosome constitution of 500 infants dying during the perinatal period. With an appendix concerning other genetic disorders among these infants

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

Chromosome constitution of 500 infants dying during the perinatal period. With an appendix concerning other genetic disorders among these infants (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

maternal health

0 references

author name string

G A Machin

1

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

J A Crolla

2

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

publication date

1 January 1974

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

23

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

3

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

183-198

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three further cases of triploidy in man surviving to birth

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human population cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid processing of primary embryonic tissues for chromosome banding pattern analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Judgment of fetal age. 3. The pathologist's evaluation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and occurrence of chromosomal syndromes: II. E-trisomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on chromosomal nondisjunction in man. 3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Post Mortem Chromosome Analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased frequency of chromosomal anomalies in abortions after induced ovulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NECROPSY SPLEEN SAMPLES FOR CHROMOSOME CULTURES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE USE OF THYMUS AND SPLEEN IN THE DEMONSTRATION OF CHROMOSOMES POSTMORTEM IN FOETUSES AND INFANTS

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival and the sex ratio in trisomy 17-18

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome aberrations in 2159 consecutive newborn babies

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple smear method for the sampling and culturing of embryonal and fetal tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHRONIC FETAL DISTRESS AND PLACENTAL INSUFFICIENCY

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anencephaly and ovulation stimulation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased brain weight-liver weight ratio as a necropsy sign of intrauterine undernutrition

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies in 5,049 consecutive newborn children

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in early spontaneous abortions

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome anomalies as a cause of spontaneous abortion

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

E (16-18) trisomy syndrome: analysis of 13 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The endometrial karyotypic profiles of women after clomiphene citrate therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XYY males in Victoria

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetics of spontaneously aborted human fetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal organ and cellular growth with various chromosomal disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Chromosome aberrations in human spontaneous abortion]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis of postmortem cultured leukocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies in a neonatal population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 17-18. A study of five cases, three of whom were associated with oesophageal atresia

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotypes of cultured cells from foetal membranes of normal newborns

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Simple Method for Postmortem Cultivation of Human Leucocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anencephaly and ovulation stimulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal anomalies in spontaneously aborted human fetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TRISOMY 18 SYNDROME WITH ABSENT RADIUS, VARUS DEFORMITY OF HAND, AND RUDIMENTARY THUMB: REPORT OF A CASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 18, Esophageal Atresia, Anomalies of the Radius, and Congenital Hypoplastic Thrombocytopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00285104

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

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=Q46391702&oldid=2109212601"