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Items: 7

1.

Prenatal cytogenetic results from cases referred for 44 different types of abnormal ultrasound findings.

Hanna JS, Neu RL, Lockwood DH.

Prenat Diagn. 1996 Feb;16(2):109-15.

PMID:
8650120
2.

Child with multiple anomalies and a group B(4-5) long arm deletion (Bq-).

Lindenbaum RH, Butler LJ.

Arch Dis Child. 1971 Feb;46(245):99-101. No abstract available.

3.

A complex familial translocation involving chromosomes 5, 9 and 13.

Fredga K, Hall B.

Cytogenetics. 1970;9(4):294-306. No abstract available.

PMID:
5474810
4.

Deletion mapping of human chromosome 5 using chromosome-specific DNA probes.

Carlock LR, Skarecky D, Dana SL, Wasmuth JJ.

Am J Hum Genet. 1985 Sep;37(5):839-52.

5.

Chromosome studies in patients with congenital malformations and mental retardation.

Erdtmann B, Salzano FM, Mattevi MS.

Humangenetik. 1975;26(4):297-306.

PMID:
1150230
6.

Cytogenetic findings in fifty-five couples with recurrent fetal wastage.

Byrd JR, Askew DE, McDonough PG.

Fertil Steril. 1977 Mar;28(3):246-50.

PMID:
557002
7.

Pure red cell hypoplasia associated with long-arm deletion of chromosome 5.

DiBenedetto J Jr, Padre-Mendoza T, Albala MM.

Hum Genet. 1979 Feb 15;46(3):345-8.

PMID:
437779

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