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Clinical Genetics
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April 1, 1983
Translocations in Prader-Willi syndrome
J Charrow, N Balkin, M M Cohen
The Journal of Craniofacial Surgery
|
January 1, 1993
Surgical treatment of patients with lobar holoprosencephaly: a personal note
J M Pensler, S Giese, J Charrow
American Journal of Medical Genetics
|
September 1, 1999
Intracranial gliomas in neurofibromatosis type 1
R Listernick, J Charrow, D H Gutmann
Clinical Genetics
|
January 1, 1985
Late onset GM2 gangliosidosis: an alpha-locus genetic compound with near normal hexosaminidase activity
J Charrow, K Inui, D A Wenger
American Journal of Diseases of Children (1960)
|
April 1, 1978
Potato craving secondary to potassium wasting in Bartter's syndrome
R S Pynoos, J Charrow, D Gribetz
American Journal of Medical Genetics
|
July 27, 2001
Comments on neurofibromatosis 1 and optic pathway tumors
R Listernick, J Charrow, D H Gutmann
American Journal of Medical Genetics
|
January 1, 1981
Duplication 3p syndrome: report of a new case and review of the literature
J Charrow, M M Cohen, D Meeker
American Journal of Human Genetics
|
July 1, 1981
Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1
M M Cohen, J Charrow, H L Nadler
The Journal of Pediatrics
|
July 1, 1994
Natural history of optic pathway tumors in children with neurofibromatosis type 1: a longitudinal study
R Listernick, J Charrow, M Greenwald, et al.
The Journal of Pediatrics
|
December 24, 1997
Neurofibromatosis type I and precocious puberty: beyond the chasm
R Habiby, B Silverman, R Listernick, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
Clinical Genetics
|
April 1, 1983
Translocations in Prader-Willi syndrome
J Charrow, N Balkin, M M Cohen
The Journal of Craniofacial Surgery
|
January 1, 1993
Surgical treatment of patients with lobar holoprosencephaly: a personal note
J M Pensler, S Giese, J Charrow
American Journal of Medical Genetics
|
September 1, 1999
Intracranial gliomas in neurofibromatosis type 1
R Listernick, J Charrow, D H Gutmann
Clinical Genetics
|
January 1, 1985
Late onset GM2 gangliosidosis: an alpha-locus genetic compound with near normal hexosaminidase activity
J Charrow, K Inui, D A Wenger
American Journal of Diseases of Children (1960)
|
April 1, 1978
Potato craving secondary to potassium wasting in Bartter's syndrome
R S Pynoos, J Charrow, D Gribetz
American Journal of Medical Genetics
|
July 27, 2001
Comments on neurofibromatosis 1 and optic pathway tumors
R Listernick, J Charrow, D H Gutmann
American Journal of Medical Genetics
|
January 1, 1981
Duplication 3p syndrome: report of a new case and review of the literature
J Charrow, M M Cohen, D Meeker
American Journal of Human Genetics
|
July 1, 1981
Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1
M M Cohen, J Charrow, H L Nadler
The Journal of Pediatrics
|
July 1, 1994
Natural history of optic pathway tumors in children with neurofibromatosis type 1: a longitudinal study
R Listernick, J Charrow, M Greenwald, et al.
The Journal of Pediatrics
|
December 24, 1997
Neurofibromatosis type I and precocious puberty: beyond the chasm
R Habiby, B Silverman, R Listernick, et al.
Page
of 5