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Results of search for 'au:"Harrod, M"', page 2 of 3
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Authors
Ardinger, H H
Brown, M S
Byrne, J B
Currarino, G
Dev, V G
Friedman, J M
Goldstein, J L
Harrod, M
Harrod, M E
Harrod, M J
Howard-Peebles, P N
Kastritsis, C D
MacDonald, P C
Madden, J D
Ott, J
Rutledge, J
Rutledge, J C
Santos-Ramos, R
Weinberg, A G
Wilson, J D
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Abnormalities, Multiple
Adolescent
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Animals
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Child, Preschool
Chromosome Aberrations
Disorders of Sex Development
Female
Genetic Counseling
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abnormalities
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genetics
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English
Your search returned 44 results.
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21.
Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment.
[electronic resource]
by
Friedman, J M
Harrod, M J
Howard-Peebles, P N
Producer:
19921006
In:
American journal of medical genetics
vol. 44
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22.
Polycystic kidney disease in a patient with the oral-facial-digital syndrome - type I.
[electronic resource]
by
Harrod, M J
Stokes, J
Peede, L F
Goldstein, J L
Producer:
19760415
In:
Clinical genetics
vol. 9
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23.
Duplication 12q mosaicism in two unrelated patients with a similar syndrome.
[electronic resource]
by
Harrod, M J
Byrne, J B
Dev, V G
Francke, U
Producer:
19810424
In:
American journal of medical genetics
vol. 7
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24.
Methotrexate and reproduction in men: case report and recommendations.
[electronic resource]
by
Morris, L F
Harrod, M J
Menter, M A
Silverman, A K
Producer:
19931119
In:
Journal of the American Academy of Dermatology
vol. 29
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25.
Familial absorptive hypercalciuria in a large kindred.
[electronic resource]
by
Pak, C Y
McGuire, J
Peterson, R
Britton, F
Harrod, M J
Producer:
19820322
In:
The Journal of urology
vol. 126
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26.
Etiologic heterogeneity of fetal hydrocephalus diagnosed by ultrasound.
[electronic resource]
by
Harrod, M J
Friedman, J M
Santos-Ramos, R
Rutledge, J
Weinberg, A
Producer:
19841003
In:
American journal of obstetrics and gynecology
vol. 150
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27.
del(20p) with manifestations of arteriohepatic dysplasia.
[electronic resource]
by
Byrne, J L
Harrod, M J
Friedman, J M
Howard-Peebles, P N
Producer:
19860917
In:
American journal of medical genetics
vol. 24
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28.
Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome.
[electronic resource]
by
Griffin, J E
Edwards, C
Madden, J D
Harrod, M J
Wilson, J D
Producer:
19760925
In:
Annals of internal medicine
vol. 85
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29.
Alginate, small bowel sterol excretion, and absorption of nutrients in ileostomy subjects.
[electronic resource]
by
Sandberg, A S
Andersson, H
Bosaeus, I
Carlsson, N G
Hasselblad, K
Härröd, M
Producer:
19941108
In:
The American journal of clinical nutrition
vol. 60
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30.
Genetic heterogeneity in spondyloepiphyseal dysplasia congenita.
[electronic resource]
by
Harrod, M J
Friedman, J M
Currarino, G
Pauli, R M
Langer, L O
Producer:
19840827
In:
American journal of medical genetics
vol. 18
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31.
Anatomic correlates of ultrasonographic prenatal diagnosis.
[electronic resource]
by
Rutledge, J C
Weinberg, A G
Friedman, J M
Harrod, M J
Santos-Ramos, R
Producer:
19860328
In:
Prenatal diagnosis
vol. 6
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32.
Ataxia and a cerebellar defect in the exencephaly-prone SELH/Bc mouse stock.
[electronic resource]
by
Juriloff, D M
Harris, M J
Harrod, M L
Gunn, T M
Miller, J E
Producer:
19930805
In:
Teratology
vol. 47
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33.
A cutaneous marker in the Hunter syndrome a report of four cases.
[electronic resource]
by
Prystowsky, S D
Maumenee, I H
Freeman, R G
Herndon, J H
Harrod, M J
Producer:
19770622
In:
Archives of dermatology
vol. 113
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34.
Familial pseudomembranous colitis and its relation to lincomycin therapy.
[electronic resource]
by
Harrod, M J
Brown, M S
Weinberg, A G
Harkness, W N
Goldstein, J L
Producer:
19751204
In:
The American journal of digestive diseases
vol. 20
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35.
Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.
[electronic resource]
by
Wilson, J D
Harrod, M J
Goldstein, J L
Hemsell, D L
MacDonald, P C
Producer:
19740605
In:
The New England journal of medicine
vol. 290
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36.
alpha-L-iduronidase deficiency and possible Hurler-Scheie genetic compound. Clinical, pathologic, and biochemical findings.
[electronic resource]
by
Winters, P R
Harrod, M J
Molenich-Heetred, S A
Kirkpatrick, J
Rosenberg, R N
Producer:
19761230
In:
Neurology
vol. 26
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37.
Fryns syndrome: prenatal diagnosis and pathologic correlation.
[electronic resource]
by
Sheffield, J S
Twickler, D M
Timmons, C
Land, K
Harrod, M J
Ramus, R M
Producer:
19981204
In:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
vol. 17
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38.
A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.
[electronic resource]
by
Rutledge, J C
Friedman, J M
Harrod, M J
Currarino, G
Wright, C G
Pinckney, L
Chen, H
Producer:
19841228
In:
American journal of medical genetics
vol. 19
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39.
Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias.
[electronic resource]
by
Walsh, P C
Madden, J D
Harrod, M J
Goldstein, J L
MacDonald, P C
Wilson, J D
Producer:
19741217
In:
The New England journal of medicine
vol. 291
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40.
Sternal malformation/vascular dysplasia association.
[electronic resource]
by
Hersh, J H
Waterfill, D
Rutledge, J
Harrod, M J
O'Sheal, S F
Verdi, G
Martinez, S
Weisskopf, B
Producer:
19850708
In:
American journal of medical genetics
vol. 21
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