Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion.

Wauters, J G

Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion. [electronic resource] - Clinical genetics Nov 1993 - 262-9 p. digital

Publication Type: Journal Article

0009-9163

10.1111/j.1399-0004.1993.tb03894.x doi


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