DNA2 gene ( OMIM ) on chromosome 10q21; SCKL9 ( OMIM ), caused by mutation in the TRAIP gene ( OMIM ) on chromosome 3p21; and SCKL10 ( OMIM ), caused by mutation in the NSMCE2
[mendelian.co]
nose, prognathism, coarse lips, halux valgum, kyphosis, lordosis p15 q36 11916331 1394 Edit 25 MCN_19940002-049 46, XX, t(7;14)(p13;q24.1) scoliosis, mental retardation,
[chr7.org]
[…] in the CEP63 gene ( OMIM ) on chromosome 3q22; SCKL7 ( OMIM ), caused by mutation in the NIN gene ( OMIM ) on chromosome 14q22; SCKL8 ( OMIM ), caused by mutation in the
[mendelian.co]