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American Journal of Medical Genetics
|
July 11, 1997
Noncompaction of the ventricular myocardium in Melnick-Needles syndrome
J A Wong, M K Bofinger
American Journal of Diseases of Children (1960)
|
August 1, 1977
Cat eye syndrome. Partial trisomy 22 due to translocation in the mother
M K Bofinger, S W Soukup
Pediatric Radiology
|
January 1, 1989
Prominent transverse (Bowdler) bone spurs as a diagnostic clue in a case of neonatal hypophosphatasia without metaphyseal irregularity
A E Oestreich, M K Bofinger
American Journal of Ophthalmology
|
June 1, 1977
Pathologic features of the eye in Down's syndrome with relationship to other chromosomal anomalies
J Ginsberg, M K Bofinger, J R Roush
American Journal of Perinatology
|
November 1, 1991
Ultrasound and genetic features of a term triploid pregnancy
S A Wasserman, M K Bofinger, L R Saldana
Clinical Genetics
|
February 1, 1978
Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygote
C H Wharton, H K Berry, M K Bofinger
Obstetrics and Gynecology
|
May 1, 1989
Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome
D J Mostello, M K Bofinger, T A Siddiqi
American Journal of Diseases of Children (1960)
|
February 1, 1982
Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria)
H K Berry, M H Hsieh, M K Bofinger, et al.
Developmental Medicine and Child Neurology
|
June 1, 1979
Intellectual development and academic achievement of children treated early for phenylketonuria
H K Berry, D J O'Grady, L J Perlmutter, et al.
Pediatric Neurology
|
May 20, 1998
Strokes, cutis marmorata telangiectatica congenita, and factor V Leiden
R A Gruppo, T J DeGrauw, S Palasis, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics
|
July 11, 1997
Noncompaction of the ventricular myocardium in Melnick-Needles syndrome
J A Wong, M K Bofinger
American Journal of Diseases of Children (1960)
|
August 1, 1977
Cat eye syndrome. Partial trisomy 22 due to translocation in the mother
M K Bofinger, S W Soukup
Pediatric Radiology
|
January 1, 1989
Prominent transverse (Bowdler) bone spurs as a diagnostic clue in a case of neonatal hypophosphatasia without metaphyseal irregularity
A E Oestreich, M K Bofinger
American Journal of Ophthalmology
|
June 1, 1977
Pathologic features of the eye in Down's syndrome with relationship to other chromosomal anomalies
J Ginsberg, M K Bofinger, J R Roush
American Journal of Perinatology
|
November 1, 1991
Ultrasound and genetic features of a term triploid pregnancy
S A Wasserman, M K Bofinger, L R Saldana
Clinical Genetics
|
February 1, 1978
Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygote
C H Wharton, H K Berry, M K Bofinger
Obstetrics and Gynecology
|
May 1, 1989
Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome
D J Mostello, M K Bofinger, T A Siddiqi
American Journal of Diseases of Children (1960)
|
February 1, 1982
Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria)
H K Berry, M H Hsieh, M K Bofinger, et al.
Developmental Medicine and Child Neurology
|
June 1, 1979
Intellectual development and academic achievement of children treated early for phenylketonuria
H K Berry, D J O'Grady, L J Perlmutter, et al.
Pediatric Neurology
|
May 20, 1998
Strokes, cutis marmorata telangiectatica congenita, and factor V Leiden
R A Gruppo, T J DeGrauw, S Palasis, et al.
Page
of 2