Terminal deletion of chromosome 1 (q43) in a female infant

Journal of Medical Genetics

Volumn 25, Issue 3, 1988, Pages 211-212

  Garani, G P ^a   Tamisari, L ^a   Volpato, S ^a   Vigi, V ^a  

^a UNIVERSITY OF FERRARA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 1Q; CHROMOSOME DELETION 1; CYTOLOGY; FEMALE; HUMAN; INFANT; MALFORMATION SYNDROME; PARTIAL MONOSOMY 1; SKIN APLASIA;

EID: 0023830612     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.25.3.211     Document Type: Article

References (4)

1. Young, R.S.; Fidone, G.S.; Reider-Garcia, P.A.; Hansen, K.L.; McCombs, J.L.; Moore, C.M. Deletions of the long arm of chromosome 6; two new cases and review of the literature Am J Med Genet 1985 10.1002/ajmg.1320200105 20 21
2. Schwartz, M.F.; Kaffe, S.; Wallace, S.; Desnick, R.J. Interstitial deletion of the long arm of chromosome 6 (del(6)(q16-q22); case report and review of the literature Clin Genet 1984 26 574
3. McNeal, R.M.; Scoglund, R.R.; Franke, U. Congenital anomalies including the VATER association in a patient with a del(6)q deletion J Pediatr 1977 10.1016/S0022-3476(77)80903-7 91 957
4. Wright, L.L.; Schwartz, M.F.; Schwartz, S.; Karesh, J. An unusual ocular finding associated with chromosome lq deletion syndrome Pediatrics 1986 77 786