Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion. [electronic resource]
Producer: 19940324Description: 262-9 p. digitalISSN:- 0009-9163
- Abnormalities, Multiple -- diagnosis
- Abortion, Therapeutic
- Chromosome Aberrations -- diagnosis
- Chromosome Disorders
- Chromosome Inversion
- Chromosomes, Human, Pair 6
- Facial Bones -- abnormalities
- Female
- Fetal Diseases -- diagnosis
- Humans
- In Situ Hybridization, Fluorescence
- Infant, Newborn
- Intellectual Disability -- genetics
- Kidney -- abnormalities
- Male
- Monosomy
- Mosaicism
- Pedigree
- Pregnancy
- Pregnancy Trimester, First
- Pregnancy Trimester, Second
- Pregnancy in Diabetics
- Prenatal Diagnosis
- Skull -- abnormalities
- Trisomy
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.