Concepedia

Author

J. M. Cant�

Mexican Social Security Institute

Also Known As

J. -M. Cant�, J. M. Cant�, J.M. Cant�

17

Publications

510

Citations

11

H-Index

28

Concepts

All Affiliations

Mexican Social Security InstituteSecretaría de Salud de JaliscoHospital Psiquiatrico Infantil Juan N NavarroHospital de Especialidades
JM

About

J. M. Cant� is an author at Mexican Social Security Institute specializing in medicine, pathology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

9

9

441

2

Health Sciences

1

1

26

3

Natural Sciences

1

1

20

4

Cell Biology

1

1

26

5

Immunology

1

1

26

J. M. Cant�

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11

Publications

483

Citations

11

H-Index

YearCitations

Inherited congenital normofunctional testicular hyperplasia and mental deficiency

J. M. Cant�, H.E. Scaglia, M Medina,

Human Genetics

1976

133

A distinct osteochondrodysplasia with hypertrichosis?Individualization of a probable autosomal recessive entity

J. M. Cant�, Diana García‐Cruz, José Sánchez‐Corona,

Human Genetics

1982

115

Inherited congenital normofunctional testicular hyperplasia and mental deficiency

J. M. Cant�, H.E. Scaglia, M. Gonz�lez-Diddi,

Human Genetics

1978

42

Pure monosomy and trisomy 2q24.2?q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations

M Möller, D. Garc�a-Cruz, Horacio Rivera,

Human Genetics

1984

31

The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation

F. Rivas, Horacio Rivera, M. L. Plascencia,

Human Genetics

1984

27

G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia

G Vaca, B Ibarra, F. Romero,

Human Genetics

1982

26

Familial true hermaphrodism in three siblings

S Armendares, F Salamanca, J. M. Cant�,

Human Genetics

1975

26

Red blood cell sorbitol dehydrogenase deficiency in a family with cataracts

G Vaca, B Ibarra, M. Bracamontes,

Human Genetics

1982

25

The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism

R. Mart�nez y Mart�nez, R Ocampo-Campos, R. P�rez-Arroyo,

European Journal of Pediatrics

1985

22

Autosomal dominant macroglossia in two unrelated families

M. C. Reynoso, A. Hern�ndez, Fernando Martínez-Pereda Soto,

Human Genetics

1986

20

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