Disease: Cantu Sanchez-Corona Garcia-cruz syndrome
- 3-M slender-boned nanism. An intrauterine growth retardation syndrome
- A distinct dominant form of microtia and conductive hearing loss
- A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance
- A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance
- A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity
- A familial case of Cantu craniofaciofronto digital syndrome
- A syndrome with mixed deafness, Mozart ear, middle and inner ear dysplasias
- Cantu syndrome and lymphoedema
- Christian's spondylo-digital syndrome: second familial case
- Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome
- Dominant inheritance of holoprosencephaly
- Faciodigitogenital (Aarskog-Scott) syndrome
- Guadalajara camptodactyly syndrome type II
- Increased adenosine deaminase activity in a patient with cartilage-hair hypoplasia
- Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies
- Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndrome
- Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations
- SED-brachydactyly and distinctive speech: report of two new cases
- Severe mental deficiency, proportionate dwarfism, and delayed sexual maturation. A distinct inherited syndrome
- Some observations on the mental deficiency, normofunctional testicular hyperplasia and fra (X) (q28) chromosome syndrome
- Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?