Inv(10)(p11.2q21.2), a variant chromosome

Human Genetics

Volumn 101, Issue 2, 1997, Pages 175-180

  Collinson, Morag N ^a   Fisher, Andrew M ^a   Walker, Jean ^b   Currie, Jane ^c   Williams, Lisa ^d   Roberts, Paul ^e  

^a SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^b Centre for Human Genetics   (United Kingdom)

^c CHURCHILL HOSPITAL   (United Kingdom)

^d BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^e ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 10P; CHROMOSOME 10Q; CLINICAL ARTICLE; FEMALE; GENE SEGREGATION; HUMAN; MALE; PERICENTRIC CHROMOSOME INVERSION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABORTION, SPONTANEOUS; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; FERTILITY; FETAL DEATH; GENETIC COUNSELING; GREAT BRITAIN; HETEROZYGOTE; HUMANS; INVERSION, CHROMOSOME; MALE; PEDIGREE; PREGNANCY; PRENATAL DIAGNOSIS; RECOMBINATION, GENETIC; VARIATION (GENETICS);

EID: 0031440465     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050609     Document Type: Article

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