Prenatal diagnosis of mosaicism for deletion 22q13.3 [1]

Prenatal Diagnosis

Volumn 21, Issue 12, 2001, Pages 1100-

  Phelan, Mary C ^a,b   Brown, Elizabeth F ^a   Curtis Rogers, R ^a,b  

^a TC Thompson Children's Hospital   (United States)

^b GREENWOOD GENETIC CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; CHROMOSOME 22Q; CHROMOSOME DELETION; DIAGNOSTIC ACCURACY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LETTER; MOSAICISM; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENE DELETION; HUMANS; MOSAICISM; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0035684258     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.195     Document Type: Letter

References (1)

1. 22q13 deletion syndrome