- MI,
Friedman JM,
Robinson WP,
Lehman A (2019)
Renpenning syndrome in a female. Am J Med
Genet A
RENPENNING H,
GERRARD JW,
ZALESKI WA,
TABATA T (November...
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INTERNATIONAL JOURNAL OF NURSING, 5(1). G., Taylor, Susan; McLaughlin.,
Renpenning,
Kathie (2001). Nursing :
concepts of practice. Mosby. ISBN 978-0323008648...
-
Fragile X
syndrome (FXS) is a
genetic disorder characterized by mild-to-moderate
intellectual disability. The
average IQ in
males with FXS is
under 55...
- RAB23-related
Carpenter syndrome Radial aplasia-thrombocytopenia
syndrome Renpenning syndrome Ritscher-Schinzel
syndrome Saethre-Chotzen
syndrome Smith-Magenis...
-
extrapyramidal signs Radioulnar synostosis-developmental delay-hypotonia
syndrome Renpenning syndrome Seckel syndrome 9
Severe X-linked
myotubular myopathy SIN3A-related...
-
Prolidase deficiency Pyknodysostosis RAB23-related
Carpenter syndrome Renpenning syndrome Restrictive dermopathy 1 RFT1-congenital
disorder of glycosylation...
-
Reactive arthritis Renal dysplasia-limb
defects syndrome Renfield syndrome Renpenning's syndrome Restless legs
syndrome Restrictive dermopathy Retinoic acid...
- PMID 30658535. S2CID 58574574. Taylor,
Susan G.;
Katherine Renpenning;
Kathie McLaughlin Renpenning (2011). Self-care Science,
Nursing Theory, and Evidence-based...
-
mutations in the
polyglutamine tract binding protein 1 gene (PQBP1)
cause Renpenning syndrome and X-linked
mental ****ation in
another family with microcephaly"...
-
vitreous (PHPV) RIPK4 AR
Popliteal pterygium syndrome (PPS) PQBP1 XLR
Renpenning's syndrome RBP4 AR
Retinal dystrophy, iris
coloboma and
comedogenic acne...
