["OSTEOGENESIS IMPERFECTA" AND ITS DIAGNOSTIC DIFFICULTIES].
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Child↗
Biomedical subjects
M LAMY
Publications and source records attributed to M LAMY.
[KLINEFELTER'S SYNDROME IN THE CHILD].
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Adolescent↗
THE MALADY OF TOULOUSE-LAUTREC.
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Achondroplasia↗
[ULCERO-HEMORRHAGIC RECTOCOLITIS IN CHILDREN].
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Child↗
TRUE HERMAPHRODITISM WITH XX-XY MOSAICISM, PROBABLY DUE TO DOUBLE FERTILIZATION OF THE OVUM.
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17-Hydroxycorticosteroids↗
[POLYDYSTROPHIC OLIGOPHRENIA].
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Adolescent↗
[RUBELLA IN THE PREGNANT WOMAN].
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Communicable Diseases↗
[THE DETECTION OF CARRIERS OF DELETERIOUS GENES].
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Albinism↗
[POLYDYSTROPHIC OLIGOPHRENIA (HEPARIN-SULFATE TYPE MUCOPOLYSACCHARIDOSIS)].
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Bone Diseases↗
[FAMILIAL ANECEPHALY AND REARRANGEMENT OF 2 13-15 CHROMOSOMES].
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Abnormalities, Severe Teratoid↗
[HERPES OF PRIMARY INVASION (HERPETIC GINGIVO-STOMATITIS IN CHILDREN)].
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Child↗
[PAPER ELECTROPHORESIS OF THE HEMOLYMPH OF SILKWORMS SUBJECTED TO VARIOUS EXPERIENCES. MODIFICATIONS OF THE PROTEINOGRAMS].
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Animals↗
A PICTORIAL REPORT ON THE EXPANDED ROLE OF ONE PROFESSIONAL NURSE.
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Humans↗
[THE EXCRETION OF FORMIMINOGLUTAMIC ACID (FIGLU) IN THE "NORMAL" INFANT AND IN STEATORRHEA CAUSED BY DISORDER OF INTESTINAL ABSORPTION].
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Avitaminosis↗
[CLINICAL AND BIOLOGICAL STUDY OF A CASE OF PHEOCHROMOCYTOMA].
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Blood Pressure↗
[PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].
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Blood Group Antigens↗
[HEREDITARY THYMIC HYPOPLASIA: ITS PLACE AND RESPONSIBILITY IN A CASE OF LYMPHOCYTIC, NORMOPLASMOCYTIC AND NORMOGLOBULINEMIC APLASIA IN AN INFANT].
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Agammaglobulinemia↗
ANENECEPHALY IN FRANCE.
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Abnormalities, Severe Teratoid↗