A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION

Overview

Journal Am J Hum Genet

Publisher Cell Press

Specialty Genetics

Date 1963 Dec 1

PMID 14097240

Citations 16

Authors

H L Cooper

R HERNITS

Affiliations

Soon will be listed here.

Citing Articles

Oral-facial-digital syndrome.

Dodge J, Kernohan D Arch Dis Child. 1967; 42(222):214-9.

PMID: 6024472 PMC: 2019705. DOI: 10.1136/adc.42.222.214.

[Chromosome analysis in primary and secondary amenorrhea using a lymphocyte culture].

NAUJOKS H, PALLASKE H Arch Gynakol. 1968; 205(2):162-84.

PMID: 5755024 DOI: 10.1007/BF00669410.

[Multiple abnormalities in a girl with a 46, XY,17q+ karyotype].

Engel W, REINWEIN H, Bombel D, Ritter H, Wolf U Humangenetik. 1968; 6(4):311-25.

PMID: 5713617

Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias).

BUHLER E, Luchsinger U, BUHLER U, Mehes K, STALDER G Humangenetik. 1970; 9(1):97-104.

PMID: 5489000 DOI: 10.1007/BF00696019.

[Elongated, submetacentric chromosome no. 1. A very rare heterozygote variant in man].

Saner B Humangenetik. 1970; 10(1):58-67.

PMID: 5449951 DOI: 10.1007/BF00297641.

References

Moorhead P, Nowell P, Mellman W, BATTIPS D, HUNGERFORD D . Chromosome preparations of leukocytes cultured from human peripheral blood. Exp Cell Res. 1960; 20:613-6. DOI: 10.1016/0014-4827(60)90138-5. View

PATAU K, THERMAN E, Inhorn S, Smith D, RUESS A . Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter. Chromosoma. 1961; 12:573-84. DOI: 10.1007/BF00328943. View

Yunis J, GORLIN R . Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome. Chromosoma. 1963; 14:146-53. DOI: 10.1007/BF00336756. View