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Literature DB >> 944530

A closer look at chromosomal inversions.

P S Moorhead.

Abstract

Mesh：

Year: 1976 PMID： 944530 PMCID： PMC1685009

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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12 in total

1. 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

2. Human Q and C chromosomal variations: distribution and incidence.

Authors: W H McKenzie; H A Lubs
Journal: Cytogenet Cell Genet Date: 1975

3. Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4.

Authors: A G Van der Linden; P L Pearson; J J Van de Kamp
Journal: Cytogenet Cell Genet Date: 1975

4. Inversion homozygosity of chromosome no. 9 in a higly inbred kindred.

Authors: D T Vine; S Yarkoni; M M Cohen
Journal: Am J Hum Genet Date: 1976-05 Impact factor: 11.025

5. A large pericentric inversion of human chromosome 8.

Authors: R Herva; A de la Chapelle
Journal: Am J Hum Genet Date: 1976-05 Impact factor: 11.025

6. Structural variation in chromosome No 9.

Authors: K Madan; M Bobrow
Journal: Ann Genet Date: 1974-06

7. Trisomy 9 mosaicism in a newborn infant with multiple malformations.

Authors: P Bowen; K L Ying; G S Chung
Journal: J Pediatr Date: 1974-07 Impact factor: 4.406

8. Pericentric inversions of human chromosomes 9 and 10.

Authors: A de la Chapelle; J Schröder; K Stenstrand; J Fellman; R Herva; M Saarni; I Anttolainen; I Tallila; L Tervilä; L Husa; G Tallqvist; E B Robson; P J Cook; R Sanger
Journal: Am J Hum Genet Date: 1974-11 Impact factor: 11.025

9. Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy.

Authors: A Schinzel; K Hayashi; W Schmid
Journal: Humangenetik Date: 1974

10. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

Authors: P W Allderdice; N Browne; D P Murphy
Journal: Am J Hum Genet Date: 1975-11 Impact factor: 11.025

10 in total

1. Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18.

Authors: V Vigi; P Maraschio; G Bosi; P Guerini; M Fraccaro
Journal: Hum Genet Date: 1977-06-10 Impact factor: 4.132

2. Familial pericentric inversion of chromosome 11 detected prenatally.

Authors: M H Russell; P Miller; A Killam
Journal: J Med Genet Date: 1982-04 Impact factor: 6.318

3. Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling.

Authors: J R Teyssier; F Bajolle
Journal: Hum Genet Date: 1980-02 Impact factor: 4.132

A closer look at chromosomal inversions.

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

2. Human Q and C chromosomal variations: distribution and incidence.

3. Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4.

4. Inversion homozygosity of chromosome no. 9 in a higly inbred kindred.

5. A large pericentric inversion of human chromosome 8.

6. Structural variation in chromosome No 9.

7. Trisomy 9 mosaicism in a newborn infant with multiple malformations.

8. Pericentric inversions of human chromosomes 9 and 10.

9. Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy.

10. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

1. Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18.

2. Familial pericentric inversion of chromosome 11 detected prenatally.

3. Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling.

4. High resolution of a small pericentric inversion of chromosome 11.

5. Familial pericentric inversion of chromosome 1 with a note on reproductive risks.

6. Pericentric inversions inv(2)(p11q13) and inv(2)(p13q11) in 2 unrelated families.

7. Pericentric inversion of chromosome 1 in three sterile brothers.

8. The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation.

9. Two pericentric inversions of human chromosome 11.

Review 10. Pericentric inversions. Problems and significance for clinical genetics.