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15 in total

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

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

2. A rapid banding technique for routine use in human and comparative cytogenetics.

Authors: K Sperling; R Wiesner
Journal: Humangenetik Date: 1972

3. Trisomy 21 in man due to maternal non-disjunction during the first meiotic division.

Authors: G Licznerski; J Lindsten
Journal: Hereditas Date: 1972 Impact factor: 3.271

4. Polymorphism in chromosome 4.

Authors: S Bardhan; D N Singh; K Davis
Journal: Clin Genet Date: 1981-07 Impact factor: 4.438

5. Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.

Authors: A P Craig-Holmes; F B Moore; M W Shaw
Journal: Am J Hum Genet Date: 1975-03 Impact factor: 11.025

6. Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter.

Authors: C G Palmer; S Schwartz; M E Hodes
Journal: Clin Genet Date: 1980-06 Impact factor: 4.438

7. Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).

Authors: J Morten; D G Harnden; S Bundey
Journal: J Med Genet Date: 1982-04 Impact factor: 6.318

8. A new genetic concept: uniparental disomy and its potential effect, isodisomy.

Authors: E Engel
Journal: Am J Med Genet Date: 1980

9. Quinacrine mustard and nucleolar organizer region heteromorphisms in twins.

Authors: C C Morton; L A Corey; W E Nance; J A Brown
Journal: Acta Genet Med Gemellol (Roma) Date: 1981

10. The status of the gene map of the human chromosomes.

Authors: V A McKusick; F H Ruddle
Journal: Science Date: 1977-04-22 Impact factor: 47.728

2 in total

1. A rare heterochromatic variant of chromosome 4.

Authors: Z Docherty; S M Bowser-Riley
Journal: J Med Genet Date: 1984-12 Impact factor: 6.318

2. De novo c.2455C>T mutation of NPR2 gene in a fetus with shortened long bones and a ventricular septal defect conceived by a mother with a fragile site at 16q22.1 and a father with a rare heterochromatic variant of chromosome 4 from Vietnam.

Authors: Thi Minh Thi Ha; Tran Thao Nguyen Nguyen; Thi Mai Ngan Nguyen; Huu Nguyen Nguyen
Journal: Mol Genet Genomic Med Date: 2021-03-13 Impact factor: 2.183

2 in total