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#194190 - WOLF-HIRSCHHORN SYNDROME; WHS
Cytogenetic locations: 12563561
Gene summaries Genetic tests Medical literature
*606026 - NEGATIVE ELONGATION FACTOR COMPLEX, MEMBER A; NELFA
Cytogenetic locations: 10199401
#619695 - RAUCH-STEINDL SYNDROME; RAUST
Cytogenetic locations: 3q29
*602952 - NUCLEAR RECEPTOR-BINDING SET DOMAIN PROTEIN 2; NSD2
Cytogenetic locations: 33941880
*604407 - LEUCINE ZIPPER/EF-HAND-CONTAINING TRANSMEMBRANE PROTEIN 1; LETM1
Cytogenetic locations: 18628306
*194648 - ZINC FINGER PROTEIN 141; ZNF141
Cytogenetic locations: 28268908
*142983 - MSH HOMEOBOX 1; MSX1
Cytogenetic locations: 19251632
#618807 - LIPOPROTEIN(a) QUANTITATIVE TRAIT LOCUS; LPAQTL
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL, INCLUDED
Cytogenetic locations: -
#107600 - APLASIA CUTIS CONGENITA, NONSYNDROMIC; ACC
Cytogenetic locations: 21614989
*600584 - NK2 HOMEOBOX 5; NKX2-5
Cytogenetic locations: 12360233
#143100 - HUNTINGTON DISEASE; HD
Cytogenetic locations: 4p16-q34
%609939 - SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6
Cytogenetic locations: 19286673
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