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#614230 - CHROMOSOME 8q21.11 DELETION SYNDROME
Cytogenetic locations: #dMn##
Gene summaries Genetic tests Medical literature
#600383 - MESOMELIA-SYNOSTOSES SYNDROME
Cytogenetic locations: previously
#618167 - OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD
Cytogenetic locations: p#####
#147891 - ISCHIOCOXOPODOPATELLAR SYNDROME WITH OR WITHOUT PULMONARY ARTERIAL HYPERTENSION; ICPPS
Cytogenetic locations: ##+###
#181270 - SCALP-EAR-NIPPLE SYNDROME; SENS
#181450 - ULNAR-MAMMARY SYNDROME; UMS
Cytogenetic locations: 612492
214290 - CERVICAL VERTEBRAE, AGENESIS OF
%174600 - POLYDACTYLY, PREAXIAL III; PPD3
133600 - EXOSTOSES OF HEEL
*614620 - INTRAFLAGELLAR TRANSPORT 140; IFT140
Cytogenetic locations: ##g###
188100 - THUMB DEFORMITY
194370 - X-RAY SENSITIVITY; XRS
%122750 - COXA VARA
264050 - PRENATAL BOWING
228200 - FEMUR-FIBULA-ULNA SYNDROME
%612554 - MYOPIA 16, AUTOSOMAL DOMINANT; MYP16
121350 - CORACOCLAVICULAR JOINT, ANOMALOUS
%185700 - SYMPHALANGISM, DISTAL
%609994 - MYOPIA 11, AUTOSOMAL DOMINANT; MYP11
Cytogenetic locations: 601324
113470 - BRACHYMESOMELIA-RENAL SYNDROME
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