A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23 [1]

American Journal of Human Genetics

Volumn 58, Issue 5, 1996, Pages 1089-1092

  Amati, P ^a   Gasparini, P ^a   Zlotogora, J ^a   Zelante, L ^a   Chomel, J C ^a   Kitzis, A ^a   Kaplan, J ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FOLLITROPIN; GONADOTROPIN; LUTEINIZING HORMONE; TESTOSTERONE;

CHROMOSOME 3Q; ECHOGRAPHY; EYELID DISEASE; FEMALE; FEMALE INFERTILITY; GENE; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HUMAN; KARYOTYPE; LETTER; MALE; MAXIMUM LIKELIHOOD METHOD; OVARY INSUFFICIENCY; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; EYELIDS; FEMALE; HUMANS; OVARIAN FAILURE, PREMATURE; PEDIGREE;

EID: 0029864808     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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