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Literature DB >> 4844640

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

G A Machin, J A Crolla.

Abstract

Entities: Disease Species

Mesh：

Year: 1974 PMID： 4844640 DOI： 10.1007/bf00285104

Source DB: PubMed Journal: Humangenetik ISSN： 0018-7348

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43 in total

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

Authors: P E POLANI; J L HAMERTON; F GIANNELLI; C O CARTER
Journal: Cytogenetics Date: 1965

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

Authors: P E Conen; B Erkman
Journal: Am J Hum Genet Date: 1966-07 Impact factor: 11.025

3. Three further cases of triploidy in man surviving to birth.

Authors: S Walker; J Andrews; N M Gregson; W Gault
Journal: J Med Genet Date: 1973-06 Impact factor: 6.318

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

Authors: H P Klinger
Journal: Cytogenetics Date: 1972

5. Post mortem chromosome analysis.

Authors: I L Yoon; B T Yoon
Journal: Cytologia (Tokyo) Date: 1971-12 Impact factor: 0.791

6. Studies on chromosomal nondisjunction in man. 3.

Authors: A Robinson; W B Goad; T T Puck; J S Harris
Journal: Am J Hum Genet Date: 1969-09 Impact factor: 11.025

7. Human population cytogenetics.

Authors: W M Court-Brown; P G Smith
Journal: Br Med Bull Date: 1969-01 Impact factor: 4.291

8. Trisomy 18.

Authors: L R Shapiro
Journal: Lancet Date: 1970-11-14 Impact factor: 79.321

9. Trisomy 18.

Authors: N G Anderson; B Smithurst; S Walsh
Journal: Lancet Date: 1970-11-21 Impact factor: 79.321

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

Authors: R L Naeye; J A Kelly
Journal: Pediatr Clin North Am Date: 1966-08 Impact factor: 3.278

18 in total

1. Chromosome anomalies of infants dying during the perinatal period and premature newborn.

Authors: N P Kuleshov
Journal: Hum Genet Date: 1976-02-29 Impact factor: 4.132

2. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.

Authors: J Boué; J L Taillemite; P Hazael-Massieux; C Léonard; A Boué
Journal: Humangenetik Date: 1975-09-20

3. Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage.

Authors: B Eiben; I Bartels; S Bähr-Porsch; S Borgmann; G Gatz; G Gellert; R Goebel; W Hammans; M Hentemann; R Osmers
Journal: Am J Hum Genet Date: 1990-10 Impact factor: 11.025

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

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

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

3. Three further cases of triploidy in man surviving to birth.

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

5. Post mortem chromosome analysis.

6. Studies on chromosomal nondisjunction in man. 3.

7. Human population cytogenetics.

8. Trisomy 18.

9. Trisomy 18.

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

1. Chromosome anomalies of infants dying during the perinatal period and premature newborn.

2. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.

3. Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage.

4. A cytogenetic study of human spontaneous abortions using banding techniques.

5. Frequency of chromosomal abnormalities in miscarriages and perinatal deaths.

6. Chromosome variation in perinatal mortality: a survey of 500 cases.

7. Trisomy 16q13----qter in a infant from a t(11;16)(q25;q13) translocation-carrier father.

8. Trisomy 16q21 = to qter.

9. Complete trisomy 9 in two liveborn infants.

10. Chromosome abnormalities in newborn children. Physical aspects.