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Journal of Medical Genetics
|
December 1, 1977
Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3)
O Sanchéz, P Mamunes, J J Yunis
Clinical Genetics
|
November 1, 1986
Spastic paresis, glaucoma and mental retardation--a probable autosomal recessive syndrome?
G Chenevix-Trench, R Leshner, P Mamunes
The Journal of Pathology
|
November 1, 1977
The pathology of Sandhoff's disease
M G Hadfield, P Mamunes, R B David
Pediatrics
|
September 1, 1980
Renal hypophosphatemic rickets: growth acceleration after long-term treatment with 1,25-dihydroxyvitamin-D3
J C Chan, R D Lovinger, P Mamunes
American Journal of Medical Genetics
|
May 1, 1983
Autosomal dominant inheritance of the Aarskog syndrome
R E Grier, F H Farrington, R Kendig, et al.
American Journal of Medical Genetics
|
April 1, 1991
Holoprosencephaly in a newborn girl with 46,XX,i(18q)
N B Spinner, D L Eunpu, J R Austria, et al.
American Journal of Medical Genetics
|
February 1, 1987
A new syndrome with features of the Smith-Lemli-Opitz and Meckel-Gruber syndromes in a sibship with cerebellar defects
A C Casamassima, P Mamunes, I M Gladstone, et al.
American Journal of Medical Genetics
|
September 14, 1999
Variability in a family with an insertion involving 5p
R C Marinescu, P Mamunes, A D Kline, et al.
Inflammatory Bowel Diseases
|
June 4, 2020
Predictors of High Health Care Utilization in Patients With Inflammatory Bowel Disease Within 1 Year of Establishing Specialist Care
Kenechukwu Chudy-Onwugaje, Alexander P Mamunes, David A Schwartz, et al.
Pediatrics
|
May 1, 1976
Intellectual deficits after transient tyrosinemia in the term neonate
P Mamunes, P E Prince, N H Thornton, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Journal of Medical Genetics
|
December 1, 1977
Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3)
O Sanchéz, P Mamunes, J J Yunis
Clinical Genetics
|
November 1, 1986
Spastic paresis, glaucoma and mental retardation--a probable autosomal recessive syndrome?
G Chenevix-Trench, R Leshner, P Mamunes
The Journal of Pathology
|
November 1, 1977
The pathology of Sandhoff's disease
M G Hadfield, P Mamunes, R B David
Pediatrics
|
September 1, 1980
Renal hypophosphatemic rickets: growth acceleration after long-term treatment with 1,25-dihydroxyvitamin-D3
J C Chan, R D Lovinger, P Mamunes
American Journal of Medical Genetics
|
May 1, 1983
Autosomal dominant inheritance of the Aarskog syndrome
R E Grier, F H Farrington, R Kendig, et al.
American Journal of Medical Genetics
|
April 1, 1991
Holoprosencephaly in a newborn girl with 46,XX,i(18q)
N B Spinner, D L Eunpu, J R Austria, et al.
American Journal of Medical Genetics
|
February 1, 1987
A new syndrome with features of the Smith-Lemli-Opitz and Meckel-Gruber syndromes in a sibship with cerebellar defects
A C Casamassima, P Mamunes, I M Gladstone, et al.
American Journal of Medical Genetics
|
September 14, 1999
Variability in a family with an insertion involving 5p
R C Marinescu, P Mamunes, A D Kline, et al.
Inflammatory Bowel Diseases
|
June 4, 2020
Predictors of High Health Care Utilization in Patients With Inflammatory Bowel Disease Within 1 Year of Establishing Specialist Care
Kenechukwu Chudy-Onwugaje, Alexander P Mamunes, David A Schwartz, et al.
Pediatrics
|
May 1, 1976
Intellectual deficits after transient tyrosinemia in the term neonate
P Mamunes, P E Prince, N H Thornton, et al.
Page
of 2